采用水基前驱溶液喷墨印刷制备光催化活性TiO2薄膜

摘译 近年来,作为一种高能量带隙半导体,二氧化钛(TiO2)由于在紫外光照射下具有良好的光催化活性,已引起科研人员的广泛关注.由于TiO2无色透明,具有广泛的应用前景,如薄的TiO2涂层可用于创建自清洁、防雾、超亲水表面.同时,也能用于太阳能电池等光电子行业. 化学溶液沉积法因具有相对简单的大面积生产工艺,且较低的制膜成本和高可用性,成为TiO2薄膜制备常用的方法之一.针对另一种TiO2制备方法,即溶胶凝胶法,大量研究文献主要关注乙醇的水解控制.然而,工业需求鼓励开发水基前驱设计.其难度在于钛醇盐与水的高反应性.在有机介质中,加入少量的水往往导致水解.因此,需要采用络合剂作为稳定剂,阻止纯水中的水解反应和避免由此产生的产物沉淀.     

Inkjet printing of photocatalytically active TiO2 thin films from water based precursor solutions

In this work, aqueous chemical solution deposition route suited for inkjet printing is used for the synthesis of photocatalytically active TiO₂ coatings. Environmentally friendly precursor solutions with electromagnetic ink-jet printing, allows cheap and simple processing of TiO₂ films on glass. The hydrolysis reaction of water sensitive titanium alkoxide (Ti-alkoxide) precursor is controlled by adding complexing agents as citric acid and triethanolamine prior to water addition, and aqueous stable solutions are achieved. The pH of the solutions is brought to neutral to guarantee flexible processing, avoid damage to substrates and equipment. Solution parameters are adapted to obtain optimal gelation conditions and good jettability. The influence of processing parameters on the phase formation and surface morphology is studied by thermogravimetric analysis and differential thermal analysis (TGA/DTA), X-ray diffraction (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The photocatalytic activity of the films is evaluated by the degradation of methyl orange.     

CHARACTERIZATION OF THE STRUCTURAL FEATURES OF OXIDIZED BEYPAZARI LIGNITE USING DECONVOLUTED SOLID STATE 13C NMR SPECTRA

ABSTRACT

The solid state ¹³C NMR method have been used to investigate the structural changes occurred in Beypazari lignite while oxidizing at 150°C in a dynamic air atmosphere. Least squares curve fitting techniques have been used to resolve the overlapping bands in the 0-220 ppm region of the 13_c NMR spectra. Measurements of the relative intensities of the functional groups observed in the oxidized coals were used to follow the progress of air oxidation. Oxidation reactions seemed to decrease the total intensities of both aliphatics and aromatics, though the reduction in aliphatics was more pronounced. The relative intensities of the total aliphatics decreased from 1.0 to 0.9 and 0.6 in the original and lignites oxidized for 12 and 312 hours, respectively. The relative intensities of Ar-C-C in the 130-148 ppm region for the same set of samples were 1.0, 0.9 and 0.8. The least-squares bands resolved in the carbonyl region were at 175 ppm and 190 ppm in the original lignite; at 180 ppm (carboxylic acids), 195 ppm (meta substituted ketones) 210 ppm (di orto substituted ketones) in the lignite oxidized for 12 hours and at 170 ppm (esters), 180 ppm, 200 ppm (aldehydes) and 210 ppm in the lignite oxidized for 312 hr. Carbonyl intensity increased from 1.0 in the original lignite to 2.3 and 3.3 in the oxidized lignites. The intensity of aromatic ethers increased from 1.0 in the original lignite to 1.9 and 1.6 for the oxidized samples. The mechanism of oxidation ether. Aldehydes are easily oxidized to carboxylic acids in the presence of air by the free radical formation of a peroxy acid. The carboxylic acid formed by disproportionation reactions between the peroxy acid and aldehydes might combine with phenols to produce esters as it was observed in the present work. The presence of high free radical concentration in the oxidation atmosphere probably caused to abstract hydrogen atoms from the aromatic structures thus degrading aromatics to produce hydroperoxides which acted later as it was described above. The gradual degradation of aromatic structures observed in the present study indicated that the oxidation reactions of the aromatic rings should less probable when compared to the oxidation of aliphatic structures.     

Influence of reducing conditions on metallic elements released from various contaminated soil samples

The redox conditions of soil may have significant consequences for the mobility of metallic elements (ME), but unlike pH, very few studies have investigated this parameter. A procedure was established to study the solubilization of ME from soil samples in various reducing conditions using a batch method and sodium ascorbate solutions. The change in redox potential from +410 to +10 mV was studied from four contaminated soil samples (designated A-D) of different origins and compositions. The results showed that ME mobilization greatly increased with decreasing redox potential within a limited and very sensitive range. Depending on the soil sample studied, various sensitive ranges of potentials were obtained (A, 220-345 mV; B, 280-365 mV; C, 260-360 mV; and D, 240-380 mV), and the induced percentages of ME mobilization varied (i.e., maximal values for Zn: A, 45%; B, 59%; C, 53%; and D, 58%). The results could be explained by the combined effect of potential and pH decrease on ME-carrying phases; in particular, Fe and Mn (oxy)hydroxides.     

Modification of the renneting process in Berridge substrate by transglutaminase

The influence of enzymatic cross‐linking on the rennet coagulation of Berridge substrate was investigated in the rennet gel samples prepared by three different methods using a microbial Tgase. Protein cross‐linking was carried out at each of three stages: before the addition of rennet, simultaneously with rennet and after the addition of rennet. The results showed that the cross‐linking of milk proteins before the addition of rennet inhibited the primary enzymatic phase of rennet coagulation. It was observed that enzymatic cross‐linking affected both the primary and the secondary phases of rennet coagulation. The most suitable application method was the addition of transglutaminase at the 5th minute after the addition of rennet.     

Characterization of microplastic deformation produced in 6061-T6 by using laser shock processing

High dislocation densities are formed in the irradiated region of the workpiece during the laser shock processing; in which case, surface hardening is resulted. The process involves with recoil pressure loading at the workpiece surface with the minimum heating effects in the irradiated region. This favors the process to be a good candidate for the surface treatment of metallic materials. Therefore, in the present study, laser shock processing of 6061-T6 aluminum alloy is carried out and the influence of a number of laser pulses and irradiated spot diameter on the treated layer characteristics, including morphology and hardness, are investigated. It is found that the number of laser pulses has significant influence on the resulting surface characteristics such as surface roughness, crystallite size, micro-strain, and microhardness of the alloy. In this case, surface roughness is deteriorated by increasing number of laser pulses and pulse intensity. In addition, fine crystallite structure takes place in the laser-treated region.     

INCIDENCE AND CHARACTERIZATION OF BACILLUS CEREUS IN MEAT AND MEAT PRODUCTS CONSUMED IN TURKEY

A total of 100 retail samples of meat and meat products were examined for Bacillus cereus using mannitol egg yolk polymyxin (MYP) agar as a selective isolation medium. Only 22.4% of the samples contained detectable levels of B. cereus, with counts ranging from log₁₀ 0.69 to 4.80 cfu/g, but a large number of other organisms up to log₁₀ 9.06 cfu/g were sometimes observed on the plates and may have masked the presence of B. cereus or inhibited growth. Two samples of soudjouck contained significant levels of B. cereus, sufficient enough to create a public health hazard. Selected isolates were tested for diarrheal enterotoxin production by a reversed passive latex agglutination (RPLA) test kit. Results showed no difference in the toxin production of B. cereus between beef, ground meat, soudjouck and pastrami samples. Plasmid‐profile analysis and susceptibility to the six commonly used antimicrobial agents were done on selected B. cereus isolates. About 96.4% of the isolates contained plasmids. Plasmid sizes ranged between 2.5 and 3.5 kb. The isolates showed a high rate of resistance to oxacillin (OXA) and amoxicillin (AMC) and a low frequency of resistance to the other antimicrobial agents, with all of them being susceptible to vancomycin (VAN). Approximately 54% of the isolates showed multiple resistance. There was no apparent relationship between drug resistance and carriage of plasmids.     

Fuel effects on Li2CuP2O7 synthesized by solution combustion method for lithium-ion batteries

Lithium copper pyrophosphate has been synthesized by the solution combustion method for the first time. Urea and hexamethylenetetramine were used as fuel. The samples were successfully prepared in low reaction temperature and short reaction time. The products were structurally characterized by FT-IR and p-XRD. Thermal behavior of samples was also investigated through TG/DT analyses. Magnetic measurements showed that the urea- and hexamethylenetetramine-assisted Li₂CuP₂O₇ were paramagnetic at room temperature. Surface analyses indicated that the fuel types changed the surface properties of samples because of exothermic redox reaction during combustion, and electrochemical performances showed clear differences. The charge capacity of urea- and hexamethylenetetramine-assisted synthesized Li₂CuP₂O₇ was calculated as 180?mAhg^?1 and 146?mAhg^?1. Synthesis method enlarged the charge capacity and prepared lithium copper pyrophosphate to have a potential for use in lithium-ion batteries.