Composition-Dependent Photoluminescence Properties and Anti-Counterfeiting Applications of A2AgX3 (A = Rb,Cs; X = Cl,Br, I)

Copper(I) halides are emerging as attractive alternatives to lead halide perovskites for optical and electronic applications. However, blue-emitting all-inorganic copper(I) halides suffer from poor stability and lack of tunability of their photoluminescence (PL) properties. Here, the preparation of silver(I) halides A₂AgX₃ (A = Rb, Cs; X = Cl, Br, I) through solid-state synthesis is reported. In contrast to the Cu(I) analogs, A₂AgX₃ are broad-band emitters sensitive to A and X site substitutions. First-principle calculations show that defect-bound excitons are responsible for the observed main PL peaks in Rb₂AgX₃ and that self-trapped excitons (STEs) contribute to a minor PL peak in Rb₂AgBr₃. This is in sharp contrast to Rb₂CuX₃, in which the PL is dominated by the emission by STEs. Moreover, the replacement of Cu(I) with Ag(I) in A₂AgX₃ significantly improves photostability and stability in the air under ambient conditions, which enables their consideration for practical applications. Thus, luminescent inks based on A₂AgX₃ are prepared and successfully used in anti-counterfeiting applications. The excellent light emission properties, significantly improved stability, simple preparation method, and tunable light emission properties demonstrated by A₂AgX₃ suggest that silver(I) halides may be attractive alternatives to toxic lead halide perovskites and unstable copper(I) halides for optical applications.     

Synthesis and characterization of epoxy based nanocomposites

Epoxy‐clay nanocomposites were synthesized to examine the effects of the content and type of different clays on the structure and mechanical properties of the nanocomposites. Diglycidyl ether of bisphenol‐A (epoxy) was reinforced by 0.5–11 wt % natural (Cloisite Na⁺) and organically modified (Cloisite 30B) types of montmorillonite. SEM results showed that as the clay content increased, larger agglomerates of clay were present. Nanocomposites with Cloisite 30B exhibited better dispersion and a lower degree of agglomeration than nanocomposites with Cloisite Na⁺. X‐ray results indicated that in nanocomposites with 3 wt % Cloisite 30B, d‐spacing expanded from 18.4 Å (the initial value of the pure clay) to 38.2 Å. The glass transition temperature increased from 73°C, in the unfilled epoxy resin, to 83.5°C in the nanocomposite with 9 wt % Cloisite 30B. The tensile strength exhibited a maximum at 1 wt % modified clay loading. Addition of 0.5 wt % organically modified clay improved the impact strength of the epoxy resin by 137%; in contrast, addition of 0.5 wt % unmodified clay improved the impact strength by 72%. Tensile modulus increased with increasing clay loading in both types of nanocomposites. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1081–1086, 2005     

Preparation of compatible blends of poly(methyl methacrylate) used in dentistry with a reactive terpolymer containing maleic anhydride and their thermomechanical characterization

This study focuses on the preparation of compatible blends with the poly(methyl methacrylate) (PMMA) using a reactive terpolymer maleic anhydride–styrene–vinyl acetate (MA–St–VA). In the first series of experiments, binary blends of the PMMA and the MA–St–VA terpolymer have been prepared in tetrahydrofurane. The PMMA and the MA–St–VA terpolymer formed the compatible blends. The effects on thermomechanical properties of MA–St–VA terpolymer ratio in the blends were studied. The glass transition temperatures (T_g), thermal expansion coefficient (α), and other thermomechanical parameters for the blends have been established by TMA method and the compatibility of two polymers has been evaluated by these TMA parameters. The addition of MA–St–VA terpolymer to PMMA made a plasticizing effect on PMMA. This effect regularly changed with the increasing of the terpolymer in the blends. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 363–367, 2006     

Operation of a frequency-narrowed high-beam quality broad-area laser by a passively stabilized external cavity technique

The average spectral bandwidth of a 2 W broad-area diode laser was narrowed to 5 GHz with wavelength tunability of up to 12 nm at a center wavelength of 790 nm with the use of a Littman-Metcalf external cavity in a displaced configuration. The use of lens and combined lens-laser transformation systems allowed precise alignment of the beam shaping optics, which led to significant improvements of the beam quality and an enhanced suppression of the free-running laser modes. We characterize the spatial beam quality of our external cavity diode laser by measuring the M2 quality factor and relate this to our measured bandwidths. Our external cavity can be configured over a range of cavity lengths and is modular in design, enabling access to a broad frequency spectrum for a wide range of applications that require high-power, narrow bandwidth operation.     

Source apportionment of PM(10) and PM(2.5) using positive matrix factorization and chemical mass balance in Izmir, Turkey

Atmospheric particulate matter (PM) fractions (PM(10) and PM(2.5)) were sampled concurrently between June 2004 and May 2005 at two sites (urban and suburban) in Izmir, Turkey. The elemental composition of PM (Al, Ba, Ca, Cd, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, Sr, V, and Zn) was determined using inductively coupled plasma-optical emission spectrometer. Elemental compositions of several PM sources were also characterized. Positive matrix factorization (PMF) and chemical mass balance modeling (CMB) were applied to determine the PM sources and their contributions to air concentrations. The major contributors to PM were fossil fuel burning, traffic emissions, mineral industries and marine salt according to the PMF results. However, undetermined parts were more than 40%. On the other hand, the contributions to PM could be determined completely by CMB, and the dominant contributor was traffic with >70% at the two sites. Fossil fuel burning, mineral industries, marine salt and natural gas-fired power plant were the minor contributors.     

The empirical estimation of tensile strength of dual‐phase steels depending on carbon content and austenitizing temperature

Surface and thin film analysis – indispensable tool for coating development and ‐production A low‐carbon (0.097 wt%) steel was annealed at 820°C for 60 min. then quenched in water to develop the desired dual phase steel (DPS) structure of martensite and ferrite. The intercritically annealed steel exhibited a microstructure of equiaxed ferrite‐martensite. Continuous yielding was observed at the stress‐strain curves. New equation was developed to predict the empirical tensile strengths of DPS. Empirical results were compared with experimental data in this study and the literature. A difference changing between ± 10% was observed for experimental and empirical results.     

Dielectric and microstructural properties of YAG:Dy3+ ceramics

Yttrium aluminium garnet(Y_3 Al_5 O_(12):YAG) singly doped with Dy3+ at different concentrations was prepared by solid state reactions using repeated heating cycles over the temperature range of 1300-1600 ℃. X-ray powder diffraction analysis confirms the presence of a well-crystallized YAG perovskite phase with cubic structure(by Rietveld refinement). The rare earth dopant is successfully integrated into the YAG host lattice without any major changes in the original structure. The temperature dependence,up to 250 ℃, of the conductivity, dielectric constant, dielectric loss, and loss tangent, at various frequencies of up to 5.0 MHz for undoped and doped crystals is compared to understand the electrical and structural characteristics. The experimental results reveal that Dy3+ dopants in YAG crystal significantly influence the conductivity, dielectric constant, and lossy mechanisms, which is probably due to the 3 d-AI ions and 4 f-Dy ions incorporated at different positions of both tetrahedral and octahedral symmetries in YAG:xDy3+ ceramics.     

Determination of Chloroanisoles and Chlorophenols in Cork and Wine by using HS‐SPME and GC‐ECD Detection

Cork taint is an off‐flavor problem in wine, the main reason being the presence of 2,4,6‐trichloroanisole (TCA) in the cork stopper. In addition to the TCA, the presence of other chloroanisole and chlorophenol family compounds (the perception limits of which are very low) can also result in, or contribute to, cork taint problem. In this study, the levels of 2,4‐dichloroanisole (DCA), 2,4,6‐trichloroanisole (TCA), 2,3,4,6‐tetrachloroanisole (TeCA), pentachloroanisole (PCA), 2,4,6‐trichlorophenol (TCP), 2,3,4,6‐tetrachlorophenol (TeCP) and penthaclorophenol (PCP) were assayed in cork stoppers (natural, agglomerated and colmate) and in red wine samples from different wineries in Turkey using HS‐SPME and GC‐ECD detection. The performance parameters for all chloroanisole and chlorophenol compounds were as follows: recovery 92.48–102.53%, R 0.992‐0.996. The LOQ values were DCA (8.4 ng/L), TCA (0.8 ng/L), TeCa (0.6 ng/L), PCP (0.8 ng/L), TCP (0.8 ng/L), TeCP (1.2 ng/L), and PCP (1.1 ng/L) respectively. In cork stoppers, the amounts of 2,4,6 TCA ranged between 5.4–130.6 ng/g. The 2,3,4,6 TeCA ranged between 1.12‐8.2 ng/g and the PCA ranged between nd (not detected)‐11.01 ng/g. In the wine samples, 2,4,6 TCA ranged between 1.42–70.2 ng/L. The 2,3,4,6 TeCA ranged between nd‐15.1 ng/L and the PCA ranged from nd‐5.16 ng/L. The results indicated that there was a significant correlation between the TCA in wines and the TCA in cork stoppers.     

The synthesis of carbon nanostructures from tea plant wastes

Tea wastes are rich in carbon, nitrogen and potassium but poor in phosphorus, which signifies that they can also be used to reduce metal oxides after they are carbonised. The tea wastes were carbonised at the first stage. The sample, which was put into a ladle with screw cap, was carbonised in a muffle furnace at 400, 500, 600, 700 and 800°C for 30, 60, 90, 120, 240, 360, 720 and 1440?min. It was determined that carbon and sulphur contents of the sample carbonised at 800°C for 1440?min were 94.68 and 0.05%, respectively. Calorific value of the same sample was 8652?cal?g^?1. It was found that with increasing temperature, carbon ratio of the carbonised samples increased and their sulphur ratio decreased from 0.39 to 0.05%. The carbonised structure was subjected to the milling process as the second stage. In the milling process, particle size of the carbon-rich sample was brought into nano size and the structure acquired the energy, required for the third stage. The amorphous carbon structure obtained after the milling process was subjected to annealing process at 1400°C as the third stage. As a result of these processes, carbon nanotubes (CNTs), carbon nano-onion structures and amorphous carbon structures were determined in the structure.     

Measurements of Thermal Conductivity Variations with Temperature for the Organic Analog of the Nonmetal–Nonmetal System: Urea–4-Bromo-2-Nitroaniline

Thermal conductivity variations with temperature for solid phases in the Urea (U)–[X] mol pct 4-bromo-2-nitroaniline (BNA) system (X = 0, 2, 45, 89.9, and 100) were measured using the radial heat flow method. From graphs of thermal conductivity variations with temperature, the thermal conductivities of the solid phases at their melting temperature and temperature coefficients for the U–[X] mol pct BNA system (X  =  0, 2, 45, 89.9, and 100) were found to be 0.26, 0.55, 0.46, 0.38, and 0.23 W/Km and 0.007781, 0.005552, 0.002058, 0.002188, and 0.002811 K^?1, respectively. The ratios of thermal conductivity of the liquid phase to thermal conductivity of the solid phase in the U–[X] mol pct BNA system (X  =  0, 2, 45, 89.9, and 100) were also measured to be 0.30, 0.44, 0.46, 0.49, and 0.51, respectively, with a Bridgman-type directional solidification apparatus at their melting temperature.