Experimental investigation of thermal performance of a double-flow solar air heater having aluminium cans

This study experimentally investigates a device for inserting an absorbing plate made of aluminium cans into the double-pass channel in a flat-plate solar air heater (SAH). This method substantially improves the collector efficiency by increasing the fluid velocity and enhancing the heat-transfer coefficient between the absorber plate and air. These types of collectors had been designed as a proposal to use aluminium materials to build absorber plates of SAHs at a suitable cost. The collector had been covered with a 4-mm single glass plate, in order to reduce convective loses to the atmosphere. Three different absorber plates had been designed and tested for experimental study. In the first type (Type I), cans had been staggered as zigzag on absorber plate, while in Type II they were arranged in order. Type III is a flat plate (without cans). Experiments had been performed for air mass flow rates of 0.03 kg/s and 0.05 kg/s. The highest efficiency had been obtained for Type I at 0.05 kg/s. Also, comparison between the thermal efficiency of the SAH tested in this study with the ones reported in the literature had been presented, and a good agreement had been found.     

Photoelectrochemical characteristics of CuO films with different electrodeposition time

This paper explores the effect of electrodeposition time on microstructure, optical, and photoelectrochemical properties of CuO films. CuO films were electrochemically deposited on tin-doped indium oxide (ITO) substrates using a Cu₂O electrodeposition method followed by annealing at 550 °C for 2 h. The electrochemical deposition was carried out at different times (300, 600, 1200, and 1800 s) utilizing a copper sulfate pentahydrate and lactic acid solution. X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) were used to perform phase and microstructure analysis. Photoluminescence (PL) studies confirmed an increase in emission intensities with increasing deposition time. In addition, a significant change was observed in photoelectrochemical properties of the film by varying the deposition time. The film deposited for 600 s showed a high photocurrent density of ?0.55 mA cm^?2 at ?0.5 V. Moreover, a lowest resistance from electrochemical impedance spectroscopy (EIS) was recorded for the films electrochemically deposited for 600 s.     

Fenton and Fenton‐like oxidation of CI Basic Yellow 51: a comparative study

When ferric ions are substituted for ferrous ions in Fenton’s reagent, the reactions which occur are called Fenton‐like reactions. This study describes the relative efficiency of Fenton (with ferrous ions) and Fenton‐like (with ferric ions) reactions for the degradation of a basic dyestuff, CI Basic Yellow 51, in aqueous solution. Comparisons were made on the basis of the observed reductions in chemical oxygen demand and visible absorption of the dye solutions at optimum reaction conditions. It was found that the Fenton process with 2.63 mm ferrous ion and 39.96 mm hydrogen peroxide at the optimum pH (3.0) eliminated 92.2% of chemical oxygen demand and 98.9% of colour in 22 min, whereas 43.2% of chemical oxygen demand and 64.6% of colour was eliminated by the Fenton‐like process within the same time period, but at pH 4. The efficiency of the latter was significantly improved (to 96.6% removal of colour and 99.7% removal of chemical oxygen demand) by an increase in temperature of 35 °C (from 15 to 50 °C), while no improvements were observed in the efficiency of the Fenton process by temperature elevations.     

Polymeric amylase nanoparticles as a new semi-synthetic enzyme system for hydrolysis of starch

α-Amylase (EC 3.2.1.1; α-d-1,4,glucan glucanohydrolase) catalyzes the hydrolysis of α-d-(1,4)-glucosidic linkages in starch, glycogen, and various malto-oligosaccharides, by releasing α-anomeric products. In this study, a novel method has been developed to prepare nanoprotein particles that carry α-amylase as a monomer by using a photosensitive microemulsion polymerization process. The nanostructured α-amylase with photosensitive features have been characterized by fluorescence spectroscopy, transmission electron microscopy (TEM) and Zeta Sizer. The fluorescence intensity of amylase nanoparticles was determined to be 658 a.u. at 610 nm and the average particle size of nanoamylase was found to be about 71.8 nm. Both free α-amylase and nanoparticles were used in the hydrolysis of starch under varying reaction conditions such as pH and temperature that affect enzyme activity and the results were compared to each other. K_m values were 0.26 and 0.87 mM and V_max values were 0.36 IU mg^? 1 and 22.32 IU mg^? 1 for nanoenzyme and free enzyme, respectively. Then, thermal stability, storage stability and reusability were investigated and according to the results, activity was preserved 60% at 60 °C; 20% at 70–80 °C temperature values and 80% after 105 days storage. Finally after 10 cycles, the activity was preserved 90% and this novel enzymatic polymeric amylase nanoparticle has showed considerable potential as reusable catalyst.     

Characterization of poly(vinylferrocenium) coated surfaces and their applications in DNA sensor technology

Poly(vinylferrocenium) (PVF⁺) modified gold (Au) electrode was developed in this study for the electrochemical sensing of deoxyribonucleic acid (DNA) hybridization based on the oxidation signals of polymer and guanine, and also for the electrochemical investigation of interaction of anticancer drug, mitomycin C (MC) and DNA immobilized onto PVF⁺ modified Au electrode. PVF⁺ modified Au electrode was prepared by electrooxidation of poly(vinylferrocene) PVF at +0.7 V versus Ag/AgCl reference electrode. The polymer modified electrode and DNA immobilized polymer modified electrode were characterized by X-ray photoelectron (XPS), Fourier transform infrared-attenuated total reflentance (FTIR-ATR) and alternating current (AC) impedance spectroscopy. For application studies, differential pulse voltammetry (DPV) technique was used.     

Use of Fenton oxidation to improve the biodegradability of a pharmaceutical wastewater

The applicability of Fenton's oxidation to improve the biodegradability of a pharmaceutical wastewater to be treated biologically was investigated. The wastewater was originated from a factory producing a variety of pharmaceutical chemicals. Treatability studies were conducted under laboratory conditions with all chemicals (having COD varying from 900 to 7000 mg/L) produced in the factory in order to determine the operational conditions to utilize in the full-scale treatment plant. Optimum pH was determined as 3.5 and 7.0 for the first (oxidation) and second stage (coagulation) of the Fenton process, respectively. For all chemicals, COD removal efficiency was highest when the molar ratio of H(2)O(2)/Fe(2+) was 150-250. At H(2)O(2)/Fe(2+) ratio of 155, 0.3M H(2)O(2) and 0.002 M Fe(2+), provided 45-65% COD removal. The wastewater treatment plant that employs Fenton oxidation followed by aerobic degradation in sequencing batch reactors (SBR), built after these treatability studies provided an overall COD removal efficiency of 98%, and compliance with the discharge limits. The efficiency of the Fenton's oxidation was around 45-50% and the efficiency in the SBR system which has two reactors each having a volume of 8m(3) and operated with a total cycle time of 1 day, was around 98%, regarding the COD removal.