Thermal analysis and measurement of a solar pond prototype to study the non-convective zone salt gradient stability

Solar ponds combine solar energy collection with long-term storage and can provide reliable thermal energy at temperature ranges from 50 to 90 °C. A solar pond consists of three distinct zones. The first zone, which is located at the top of the pond and contains the less dense saltwater mixture, is the absorption and transmission region, also known as the upper convective zone (UCZ). The second zone, which contains a variation of saltwater densities increasing with depth, is the gradient zone or non-convective zone (NCZ). The last zone is the storage zone or lower convective zone (LCZ). In this region, the density is uniform and near saturation. The stability of a solar pond prototype was experimentally performed. The setup is composed of an acrylic tube with a hot plate emulating the solar thermal energy input. A study of various salinity gradients was performed based on the Stability Margin Number (SMN) criterion, which is used to satisfy the dynamic stability criterion. It was observed that erosion of the NCZ was accelerated due to mass diffusion and convection in the LCZ. It can be determined that for this prototype the density of the NCZ is greatly affected as the SMN reaches 1.5.     

Influence of ionic pretreatment on the performance of solid electrolyte dye-sensitized solar cells

Dye-sensitized solar cells (DSSCs) were manufactured with liquid iodine/iodide electrolyte solution in acetonitrile and a solid electrolyte based on plasticized poly(ethylene oxide) (PEO). Two types of titania electrodes manufactured from two-ingredient precursors were used to assess the efficacy of the solid electrolyte and the improvement produced by two chemical treatments. Solid electrolyte devices with a liquid electrolyte pretreatment applied to the electrolyte-oxide interface demonstrated improved photovoltaic performance compared to untreated solid electrolyte devices and solid electrolyte devices given an electrode-bulking sol treatment. Devices using electrodes made from hydrothermally synthesized titanate nanotubes resulted in lower performance than those made from the typically-used titania nanopowder, with significant performance loss resulting from the substitution of solid for liquid electrolyte, indicating the critical dependence of performance on electrolyte infiltration into the oxide layer.     

光电能及其效益

南非目前正开展一项崭新而雄心勃勃的计划－改善偏远农村地区的能源供应状况。该计划的一个重要组成就是授予７家私营协营体特许权,分别在不同地区安装３５万台家用太阳能光电系统。该项计划对于农村地区能源发展具有突破性的意义。     

In situ atomic oxygen erosion study of fluoropolymer films using X‐ray photoelectron spectroscopy

The surfaces of a homologous series of fluoropolymers were characterized in situ using X‐ray photoelectron spectroscopy before and after a 15‐min exposure to the flux produced by a unique hyperthermal atomic oxygen (AO) source, which produces a flux of about of 10¹⁵ atoms cm^?2 s^?1. The linear polymers investigated in this study include high‐density polyethylene (HDPE), poly(vinyl fluoride) (PVF), poly(vinylidene fluoride) (PVdF), and poly(tetrafluoroethylene) (PTFE). They possess a similar base structure with increasing fluorine‐to‐carbon ratios of 0, 1 : 2, 1 : 1, and 2 : 1, respectively. No interaction of the AO with the nonfluorine‐containing linear polymer HDPE was detected over this short exposure. However, a correlation exists between the chemical composition of the fluorinated polymers and the induced chemical and structural alterations occurring in the near‐surface region as a result of exposure to AO. The data indicate that AO initially attacks the fluorine portion of the polymers, resulting in a substantial decrease in the near‐surface fluorine concentration. The near‐surface fluorine‐to‐carbon ratios of PVF, PVdF, and PTFE decreased during the 15‐min AO exposure by 68, 39, and 18.5%, respectively. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1977–1983, 2004     

Imidazolium-Based Stabilization of Aqueous Multiwall Carbon Nanotube Dispersions

Imidazolium bromide, an ionic liquid surfactant acrylate, as well as its homopolymer and various copolymers are demonstrated to be superior dispersing aids for preparing aqueous multiwall carbon nanotube (MWCNT) dispersions. We demonstrate apparent complete exfoliation in water with extinction coefficients at 500 nm of about 60 cm² mg⁻¹ of MWCNT dispersed, a new lower bound and the highest reported extinction to date. The efficacy or efficiency of dispersion (activated by ultrasonication) is examined in terms of a quotient of extinction and weight ratio of the active monomer and MWCNT. A rank ordering of the results obtained for seven stabilizers based on the same imidazolium bromide monomer provides insights into roles of π-overlap adsorption onto MWCNT surfaces and how hydrogel properties of some of these polymers provide stability in water at higher concentrations than previously considered feasible for surfactant-stabilized and polymer-stabilized MWCNT dispersions. Simple nanocomposite film formation is demonstrated by casting and thermal diffusivity and electrical conductivity properties are examined.     

Modulation of Induced Cytotoxicity of Doxorubicin by Using Apoferritin and Liposomal Cages

Doxorubicin is an effective chemotherapeutic drug, however, its toxicity is a significant limitation in therapy. Encapsulation of doxorubicin inside liposomes or ferritin cages decreases cardiotoxicity while maintaining anticancer potency. We synthesized novel apoferritin- and liposome-encapsulated forms of doxorubicin (“Apodox” and “lip-8-dox”) and compared its toxicity with doxorubicin and Myocet on prostate cell lines. Three different prostatic cell lines PNT1A, 22Rv1, and LNCaP were chosen. The toxicity of the modified doxorubicin forms was compared to conventional doxorubicin using the MTT assay, real-time cell impedance-based cell growth method (RTCA), and flow cytometry. The efficiency of doxorubicin entrapment was 56% in apoferritin cages and 42% in the liposome carrier. The accuracy of the RTCA system was verified by flow-cytometric analysis of cell viability. The doxorubicin half maximal inhibition concentrations (IC₅₀) were determined as 170.5, 234.0, and 169.0 nM for PNT1A, 22Rv1, and LNCaP, respectively by RTCA. Lip8-dox is less toxic on the non-tumor cell line PNT1A compared to doxorubicin, while still maintaining the toxicity to tumorous cell lines similar to doxorubicin or epirubicin (IC₅₀ = 2076.7 nM for PNT1A vs. 935.3 and 729.0 nM for 22Rv1 and LNCaP). Apodox IC₅₀ was determined as follows: 603.1, 1344.2, and 931.2 nM for PNT1A, 22Rv1, and LNCaP.     

Epilepsia partialis continua: a new manifestation of anti-Hu-associated paraneoplastic encephalomyelitis

We report on 3 anti-Hu-positive patients who presented with clinical and electroencephalographic (EEG) features of epilepsia partialis continua (EPC). Two of the patients had an associated small cell carcinoma. Magnetic resonance imaging (MRI) disclosed a hyperintense nonenhancing focal lesion in T2-weighted images in the sensorimotor area in 2 patients. Histopathological analysis of the lesion revealed inflammatory infiltrates and neuronal cell loss. In the patient who had a postmortem study, these neuropathological changes were not observed in other areas of the nervous system. This study emphasizes that the possibility of an anti-Hu-associated paraneoplastic disorder must be considered in patients with cortical encephalitis presenting with EPC when a brain tumor can be excluded.     

Ground-Fault Protection of Electrical Systems with Emergency or Standby Power

Providing reliable ground-fault protection in electrical systems having alternate emergency or standby power can present serious problems unless adequate equipment is selected and properly coordinated. Multiple neutral-to-ground connections may prevent adequate sensing of ground-fault currents and may also cause nuisance tripping of circuit breakers. This paper discusses various approaches that have been proposed to solve these problems. Particular emphasis is placed on code requirements and overall reliability of the electrical systems.     

Reduction of polyhalogenated methanes by surface-bound Fe(II) in aqueous suspensions of iron oxides

Uptake of ferrous iron from aqueous solution by iron oxides results in the formation of a variety of reactive surface species capable of reducing polyhalogenated methanes (PHMs). Pseudo-first-order reaction rate constants, k(obs), of PHMs increased in the order CHBrCl2 < CHBr2Cl < CHBr3 < CCl4 < CFBr3 < CBrCl3 < CBr2Cl2. The k(obs) values increased with the exposure time, teq, of Fe(II) to suspended iron oxides which was attributed to the rearrangement of initially sorbed Fe(II) species to more reactive surface species with time. At pH 7.2, the k(obs) values of PHMs also increased with the concentration of surface-bound ferrous iron, Fe(II)sorb, particularly when Fe(II)tot was increased to concentrations where surface precipitation becomes likely. At fixed total Fe(II) concentrations, k(obs) values increased exponentially with pH. The highest reactivities were associated with pH conditions where surface precipitation of Fe(II) is expected. Fe(II)sorb and pH, however, had opposite effects on the product formation of PHMs. At pH 7.2, the formation of formate from CX4 (X = CI, Br) increased with Fe(II)sorb, whereas increasing pH favored the formation of CHX3. The ratio of halogenated products and formate formed is indicative of the relative importance of initial one- or two-electron-transfer processes, respectively, and was found to depend on the type of iron oxide mineral also. Our data form a basis to assess the importance of chemical reactions in natural attenuation processes of PHMs in environmental systems under iron-reducing conditions.