Photoinduced electron transfer mechanism between green fluorescent protein molecules and metal oxide nanoparticles

Green fluorescent protein (GFP) molecules are attached to titanium dioxide and cadmium oxide nanoparticles via sol–gel method and fluorescence dynamics of such a protein–metal oxide assembly is investigated with a conventional time correlated single photon counting technique. As compared to free fluorescent protein molecules, time-resolved experiments show that the fluorescence lifetime of GFP molecules bound to these metal oxide nanoparticles gets shortened dramatically. Such a decrease in the lifetime is measured to be 22 and 43 percent for cadmium oxide and titanium dioxide respectively, which is due to photoinduced electron transfer mechanism caused by the interaction of GFP molecules (donor) and metal oxide nanoparticles (acceptor). Our results yield electron transfer rates of 3.139×10⁸ s⁻¹ and 1.182×10⁸ s⁻¹ from the GFP molecules to titanium dioxide and cadmium oxide nanoparticles, respectively. The electron transfer rates show a marked decrease with increasing driving force energy. This effect represents a clear example of the Marcus inverted region electron transfer process.     

Thermal degradation characteristic of Tetra Pak panel boards under inert atmosphere

hermal degradation characteristics of Tetra Pak panel boards (TPPB) can be useful to improve usage of such panels as an alternative to wood-based products such as plywood, fiberboard, and particleboard. In the study, samples from the TPBBs manufactured from waste Tetra Pak packages (WTPP) were heated in a nitrogen atmosphere at different heating rates (10, 15 and 20 °C/min) using a thermal analysis system. The Coats-Redfern kinetic model was applied to calculate kinetic parameters. The degradation rate equations were then established. In addition, the kinetic compensation effect (KCE) was used to correlate the pre-exponential factor (k _o ) with activation energy (E _a ) and the existence of the KCE was accepted. TG-FT/IR analyses were applied to the TPPB degradation and then the FT-IR stack plot was used to analyze gas products (CO₂, CH₄, HCOOH, and CH₃OH). Infrared vibrational frequencies and the micro, crystal structure of the TPPBs were investigated by Fourier transform infrared spectroscopy (FT-IR), Scanning electron microscope (SEM) and X-Ray diffraction analysis (XRD), respectively.     

Parametric investigation on anhydrous sodium metaborate (NaBO2) synthesis from concentrated tincal

In this study, anhydrous sodium metaborate (NaBO₂), an industrial and technologically important boron compound, synthesis from concentrated tincal (CT) was carried out. Experiments with different temperature and time were performed in the parametric investigation to map out the reaction mechanism. Crystalline phase characterization of metaborates products indicates that anhydrous NaBO₂ synthesis from CT occurred at 400 °C with 5 h of reaction conditions. At the end of synthesis, the obtained anhydrous NaBO₂ product can be used in many fields without having the calcination step due to the advantages of this method.     

Mn(II), Co(II) and Ni(II) complexes of 4-(2-thiazolylazo)resorcinol: Syntheses, characterization, catalase-like activity, thermal and electrochemical behaviour

Manganese(II), cobalt(II) and nickel(II) acetates react with the ligand, 4-(2-thiazolylazo)resorcinol, to form complexes of general formula [ML₂] for MCo(II), Ni(II) and [ML₂]·2H₂O for MMn(II). Each of the azo complexes was characterized using elemental analysis, electrolytic conductance, UV–visible spectroscopy and magnetic susceptibility. An octahedral structure is proposed for all complexes prepared, which molar conductance data revealed to be non-electrolytes. IR spectra reveal that the ligand is coordinated to the metal ions in a tridentate manner via the resorcinol OH, azo N and thiazole N groups as donor sites. The electrochemical behaviour of the ligand and its complexes were obtained by cyclic voltammetry. Thermal decomposition studies were undertaken to secure additional information on the structure of the investigated compounds. The manganese(II) complex catalysed the disproportionation of hydrogen peroxide in the presence of imidazole.     

The analysis of corrosion performance of car bodies coated by no nickel and low nickel zinc phosphating processes

In today's automotive industry in order to protect car bodies from corrosion, spray or immersion type zinc phosphating processes are applied. In both types, nickel and chromium are widely used though they are harmful to human health and environment. In this study, car body's corrosion performance, coated by no nickel (0 ppm) and low nickel (100, 200, 300 ppm) immersion type zinc phosphating (without chromium passivation) processes, are compared to the bodies that are coated by spray and immersion type processes including nickel (500–700 ppm) and chromium. After analyzing coating weight, composition, morphology of the crystals and salt spray test corrosion performance of car bodies specimens coated by no nickel and low nickel processes are as good as the ones coated by spray and immersion phosphating processes including nickel and chromium. In developing environment consciousness, it is inevitable to favor no nickel or low nickel processes since they give no harm to nature and human health.     

Pb(II) and Cd(II) removal from aqueous solutions by olive cake

The removal of heavy metals from wastewater using olive cake as an adsorbent was investigated. The effect of the contact time, pH, temperature, and concentration of adsorbate on adsorption performance of olive cake for Pb(II) and Cd(II) ions were examined by batch method. Adsorption of Pb(II) and Cd(II) in aqueous solution onto olive cake was studied in single component. After establishing the optimum conditions, elution of these ions from the adsorbent surface was also examined. The optimum sorption conditions were determined for two elements. Maximum desorption of the Pb(II) and Cd(II) ions were found to be 95.92 and 53.97% by 0.5M HNO(3) and 0.2M HCl, respectively. The morphological analysis of the olive cake was performed by the scanning electron microscopy (SEM).     

Microwave assisted green chemistry approach of sodium metaborate dihydrate (NaBO2·2H2O) synthesis and use as raw material for sodium borohydride (NaBH4) thermochemical production

In the present study, a novel microwave assisted method has been developed for sodium metaborate dihydrate (NaBO₂·2H₂O) synthesis. Anhydrous NaBO₂, a derivative of borax, is an industrially and technologically important boron compound used as a raw material for the thermochemical production of sodium borohydride (NaBH₄). The effects of different microwave treatment conditions such as microwave power (90, 270 and 360 W) and irradiation time (1, 2, and 5 min) on the synthesis of NaBO₂·2H₂O were examined. After microwave irradiation at 270 W for 1 min, NaBO₂ crystals with 2 molar equivalents of water were formed. Anhydrous NaBO₂ was obtained following incubation at 400 °C for 33 min under calcination conditions. Then the resulting anhydrous NaBO₂ powder was reacted with MgH₂ under 60 bar hydrogen atmosphere at 470 °C, leading to successful production of NaBH₄ with 93% yield.     

Liquefaction/Solubilization of Low-Rank Turkish Coals by White-Rot Fungus (Phanerochaete chrysosporium)

Microbial coal liquefaction/solubilization of three low-rank Turkish coals (Bursa-Kestelek, Kütahya-Seyitömer and Mu?la-Yata?an lignite) was attempted by using a white-rot fungus (Phanerochaete chrysosporium DSM No. 6909); chemical compositions of the products were investigated. The lignite samples were oxidized by nitric acid under moderate conditions and then oxidized samples were placed on the agar medium of Phanerochaete chrysosporium. FTIR spectra of raw lignites, oxidized lignites and liquid products were recorded, and the acetone-soluble fractions of these samples were identified by GC-MS technique. Results show that the fungus affects the nitro and carboxyl/carbonyl groups in oxidized lignite sample, the liquid products obtained by microbial effects are the mixture of water-soluble compounds, and show limited organic solubility.     

DETERMINATION OF THE EFFECT OF LEMON ADDITION UPON ELEMENT CONCENTRATIONS IN TEA

Consumption of tea is a popular tradition in Turkey. In this article, non essential and toxic element concentrations were determined in infusions and lemon added infusions in widely consumed Turkish teas (black, earl grey, and green tea). Element concentrations were found to be in the order of aluminum > nickel > barium in black and earl grey teas. In green tea, the order was changed to aluminum > nickel > lead > barium. The concentrations of arsenic and antimony were below the detection limit of the inductively coupled plasma optical emission spectrometry method employed. The addition of lemon increased aluminum, cadmium, and lead concentrations in all teas whereas nickel concentration increased in black and green tea but decreased in earl grey. The barium concentration was same at all tea samples. In comparison with the recommended daily allowance ratios, the amount of aluminum consumed is between 13.167–24.396% in males and 17.556–32.528% in females for people who consume 200 mL of teas daily. Other elements (cadmium, lead, nickel, barium) which are a concern for tea consumption were determined and the hazard index of daily tea drinking was found to be in the safe range except for green tea with lemon addition.     

Decreased Serum Levels of Sphingomyelins and Ceramides in Sickle Cell Disease Patients

Limited data are available on the serum levels of different sphingomyelin (CerPCho) and ceramide (CER) species in sickle‐cell disease (SCD). This study was aimed at identifying the levels of C16–C24 CerPCho and C16–C24 CER in serum obtained from SCD patients and controls. Circulating levels of neutral sphingomyelinase (N‐SMase) activity, ceramide‐1‐phosphate (C1P), and sphingosine‐1‐phosphate (S1P) were also determined. Blood was collected from 35 hemoglobin (Hb)A volunteers and 45 homozygous HbSS patients. Serum levels of C16–C24 CerPCho and C16–C24 CER were determined by an optimized multiple reaction monitoring (MRM) method using ultrafast liquid chromatography (UFLC) coupled with tandem mass spectrometry (MS/MS). Serum activity of N‐SMase was assayed by standard kit methods, and C1P and S1P levels were determined by enzyme‐linked immunosorbent assay. A significant decrease was observed in the serum levels of C18–C24 CerPCho in patients with SCD compared to controls. No significant difference was found in C16 CerPCho levels between the two groups. Very‐long‐chain C22–C24 CER were significantly decreased in SCD, while long‐chain C16–C20 CER levels showed no significant difference between SCD patients and controls. Significant positive correlation was found between the serum total cholesterol levels and C18–C24 CerPCho and C22–C24 CER in SCD patients. Patients with SCD had significantly elevated serum activity of N‐SMase as well as increased circulating levels of C1P and S1P compared to controls. The decrease in serum levels of C18–C24 CerPCho in patients with SCD was accompanied by decreased levels of C22–C24 CER. Future studies are needed to understand the role of decreased CerPCho and CER in the pathophysiology of SCD.