Measurement of Occupational Eye and Thyroid Radiation Doses in Pediatric Interventional Cardiologists at a Tertiary Hospital.

Background Advances in imaging techniques have led to increased utilization of imaging devices in catheterization laboratories. Invasive surgical procedures for cardiac disorders have been largely replaced by fluoroscopic cardiac catheterization. With this increase, concerns and risks associated with exposure to ionizing radiation among interventional cardiologists are growing. This study aims to measure and compare the occupational doses to the eye lens and thyroid of pediatric interventional cardiologists during different procedures in the catheterization laboratory and its significance. Methodology In this study, cardiologists wore bandanas with attached dosimeters to measure the absorbed doses to the eyes and thyroid gland. The dosimeters were collected for reading. The procedure types were also collected. In addition, the total fluoroscopy time and tube voltage of the biplane machine were measured. SPSS version 23 (IBM Corp., Armonk, NY, USA) was used to analyze the data. The characteristics of the study sample were described using simple counts and percentages, whereas means and standard deviations were used for continuous variables. Statistical significance was set at p-values <0.05. Results A total of 93 procedures were evaluated. The mean absorbed doses for all 93 procedures in both eyes and thyroid were 0.09 mGy and 0.08 mGy, respectively. A significant difference was found between the left and right eye measurements (p = 0.034), with higher doses administered to the left eye. However, no significant difference was observed between the right and left thyroid doses (p = 0.281). Significant correlations were found between the eye and thyroid doses and the procedure type (p = 0.02 and p = 0.009, respectively). Conclusions A significant amount of radiation was measured in the measurements of both organs. In addition, radiation dose measurements varied between different types of procedures. Our current results indicate the importance and necessity of applying the radiation protection concept of dose optimization.

Effect of Adding Gadolinium Oxide Promoter on Nickel Catalyst over Yttrium-Zirconium Oxide Support for Dry Reforming of Methane.

The dry reforming of methane (DRM) was studied for seven hours at 800 °C and 42 L/(g·h) gas hourly space velocity over Ni-based catalysts, promoted with various amounts of gadolinium oxide (x = 0.0, 1.0, 2.0, 3.0, 4.0, and 5.0 wt.%) and supported on mesoporous yttrium-zirconium oxide (YZr). The best catalyst was found to have 4.0 wt.% of gadolinium, which resulted in ∼80% and ∼86% conversions of CH4 and CO2, respectively, and a mole ratio of ∼0.90 H2/CO. The addition of Gd2O3 shifted the diffraction peaks of the support to higher angles, indicating the incorporation of the promoter into the unit cell of the YZr support. The Gd2O3 promoter improved the catalyst basicity and the interaction of NiO with support, which were reflected in the coke resistance (6.0 wt.% carbon deposit on 5Ni+4Gd/YZr; 19.0 wt.% carbon deposit on 5Ni/YZr) and the stability of our catalysts. The Gd2O3 is believed to react with carbon dioxide to form oxycarbonate species and helps to gasify the surface of the catalysts. In addition, the Gd2O3 enhanced the activation of CH4 and its conversion on the metallic nickel sites.

Stability and Activity of Rhodium Promoted Nickel-Based Catalysts in Dry Reforming of Methane.

The rhodium oxide (Rh2O3) doping effect on the activity and stability of nickel catalysts supported over yttria-stabilized zirconia was examined in dry reforming of methane (DRM) by using a tubular reactor, operated at 800 °C. The catalysts were characterized by using several techniques including nitrogen physisorption, X-ray diffraction, transmission electron microscopy, H2-temperature programmed reduction, CO2-temperature programmed Desorption, and temperature gravimetric analysis (TGA). The morphology of Ni-YZr was not affected by the addition of Rh2O3. However, it facilitated the activation of the catalysts and reduced the catalyst's surface basicity. The addition of 4.0 wt.% Rh2O3 gave the optimum conversions of CH4 and CO2 of ~89% and ~92%, respectively. Furthermore, the incorporation of Rh2O3, in the range of 0.0-4.0 wt.% loading, enhanced DRM and decreased the impact of reverse water gas shift, as inferred by the thermodynamics analysis. TGA revealed that the addition of Rh2O3 diminished the carbon formation on the spent catalysts, and hence, boosted the stability, owing to the potential of rhodium for carbon oxidation through gasification reactions. The 4.0 wt.% Rh2O3 loading gave a 12.5% weight loss of carbon. The TEM images displayed filamentous carbon, confirming the TGA results.

Effect of Holmium Oxide Loading on Nickel Catalyst Supported on Yttria-Stabilized Zirconia in Methane Dry Reforming.

The carbon dioxide reforming of methane has attracted attention from researchers owing to its possibility of both mitigating the hazards of reactants and producing useful chemical intermediates. In this framework, the activity of the nickel-based catalysts, supported by yttria-stabilized zirconia and promoted with holmium oxide (Ho2O3), was assessed in carbon dioxide reforming of methane at 800 °C. The catalysts were characterized by N2-physisorption, H2 temperature-programmed reduction, temperature-programmed desorption of CO2, X-ray diffraction, scanning electron microscopy (SEM) together with energy-dispersive X-ray spectroscopy, transmission electron microscopy (TEM), and thermogravimetric analysis (TGA) techniques. The effect of holmium oxide weight percent loading (0.0, 1.0, 2.0, 3,0, 4.0, and 5.0 wt %) was examined owing to its impact on the developed catalysts. The optimum loading of Ho2O3 was found to be 4.0 wt %, where the methane and carbon dioxide conversions were 85 and 91%, respectively. The nitrogen adsorption-desorption isotherms specified the mesoporous aspect of the catalysts, while the SEM images displayed a morphology of agglomerated, porous particles. The TEM images of the spent catalyst displayed the formation of multiwalled carbon nanotubes. TGA of the 4.0 wt % of Ho2O3 catalyst, experimented over 7-hour time-on-stream, displayed little weight loss (<14.0 wt %) owing to carbon formation, indicating the good resistance of the catalyst to carbon accumulation due to the enhancing ability of Ho2O3 and its adjustment of the support.

Utilization of Incense Stick Ash in Hydrometallurgy Methods for Extracting Oxides of Fe, Al, Si, and Ca.

With rapid industrialization, there is an ever-increasing demand for iron oxides, calcium oxides, aluminum oxides, silica, and zeolites as raw materials for various industries, but reserves of such metal oxides are continuously diminishing. Therefore, there is an urgent need to explore new alternatives for such value-added minerals. One such material is incense stick ash (ISA), which is among the most unexplored byproducts from residential and holy places. Currently, ISA is of no use and it is disposed of in millions of tons (MTs) in rivers and other water bodies in India due to its sacred value. The major chemical composition of ISA is calcium, silica, alumina, ferrous minerals, magnesium, and traces of Na, K, P, Ti, etc. Major fractions of ISA, i.e., 50-60%, are made up of calcium and magnesium oxides; 20-30% of ISA is made up of silica, alumina, and ferrous minerals, as revealed by X-ray fluorescence spectroscopy (XRF). In the present research work, methods of recovery of value-added micro and nano minerals from ISA are suggested, using cost-effective techniques and an eco-friendly approach. Firstly, magnetic fractions were recovered by a magnetic separation method; then, alumina, silica, and calcium oxides were synthesized from non-magnetic fractions. The confirmation of the synthesized and extracted nanomaterials was done by Fourier transform infrared spectroscopy (FTIR), particle size analyzer (PSA), X-ray diffraction (XRD), field emission scanning electron microscopy with electron diffraction spectroscopy (FESEM-EDS), and transmission electron microscopy (TEM). The purity of synthesized particles varied from 40-80%. In the future, ISA will prove to be an alternative resource material for Fe, Ca, Si, C, Al, and zeolites, which will minimize solid waste pollution and water pollution arising due to the disposal of ISA into water bodies.

Lithium-Based Upconversion Nanoparticles for High Performance Perovskite Solar Cells.

In this work, we report an easy, efficient method to synthesize high quality lithium-based upconversion nanoparticles (UCNPs) which combine two promising materials (UCNPs and lithium ions) known to enhance the photovoltaic performance of perovskite solar cells (PSCs). Incorporating the synthesized YLiF4:Yb,Er nanoparticles into the mesoporous layer of the PSCs cells, at a certain doping level, demonstrated a higher power conversion efficiency (PCE) of 19%, additional photocurrent, and a better fill factor (FF) of 82% in comparison to undoped PSCs (PCE = ~16.5%; FF = 71%). The reported results open a new avenue toward efficient PSCs for renewable energy applications.

Promotional effect of magnesium oxide for a stable nickel-based catalyst in dry reforming of methane.

The generation of synthesis gas (hydrogen and carbon monoxide mixture) from two global warming gases of carbon dioxide and methane via dry reforming is environmentally crucial and for the chemical industry as well. Herein, magnesium-promoted NiO supported on mesoporous zirconia, 5Ni/xMg-ZrO2 (x = 0, 3, 5, 7 wt%) were prepared by wet impregnation method and then were tested for syngas production via dry reforming of methane. The reaction temperature at 800 °C was found more catalytically active than that at 700 °C due to the endothermic feature of reaction which promotes efficient CH4 catalytic decomposition over Ni and Ni-Zr interface as confirmed by CH4-TSPR experiment. NiO-MgO solid solution interacted with ZrO2 support was found crucial and the reason for high CH4 and CO2 conversions. The highest catalyst stability of the 5Ni/3Mg-ZrO2 catalyst was explained by the ability of CO2 to partially oxidize the carbon deposit over the surface of the catalyst. A mole ratio of hydrogen to carbon monoxide near unity (H2/CO ~ 1) was obtained over 5Ni/ZrO2 and 5Ni/5Mg-ZrO2, implying the important role of basic sites. Our approach opens doors for designing cheap and stable dry reforming catalysts from two potent greenhouse gases which could be of great interest for many industrial applications, including syngas production and other value-added chemicals.

Ordered Macro/Mesoporous TiO2 Hollow Microspheres with Highly Crystalline Thin Shells for High-Efficiency Photoconversion.

Well ordered, uniform 3D open macro/mesoporous TiO2 hollow microspheres with highly crystalline anatase thin shells have been successfully synthesized by a simple solvent evaporation-driven confined self-assembly method. The 3D open macro/mesoporous TiO2 hollow microspheres show high energy-conversion efficiency (up to 9.5%) and remarkable photocatalytic activity (with photodegradation of 100% for methylene blue in 12 min under UV light irradiation).

Radially oriented mesoporous TiO2 microspheres with single-crystal-like anatase walls for high-efficiency optoelectronic devices.

Highly crystalline mesoporous materials with oriented configurations are in demand for high-performance energy conversion devices. We report a simple evaporation-driven oriented assembly method to synthesize three-dimensional open mesoporous TiO2 microspheres with a diameter of ~800 nm, well-controlled radially oriented hexagonal mesochannels, and crystalline anatase walls. The mesoporous TiO2 spheres have a large accessible surface area (112 m(2)/g), a large pore volume (0.164 cm(3)/g), and highly single-crystal-like anatase walls with dominant (101) exposed facets, making them ideal for conducting mesoscopic photoanode films. Dye-sensitized solar cells (DSSCs) based on the mesoporous TiO2 microspheres and commercial dye N719 have a photoelectric conversion efficiency of up to 12.1%. This evaporation-driven approach can create opportunities for tailoring the orientation of inorganic building blocks in the assembly of various mesoporous materials.

Crystal structure of cyclo-hexyl-ammonium thio-cyanate.

In the title salt, C6H11NH3 (+)·SCN(-), the cyclo-hexyl-ammonium ring adopts a slightly distorted chair conformation. The ammonium group occupies an equatorial position to minimize 1,3 and 1,5 diaxial inter-actions. In the crystal, the components are linked by N-H⋯N and N-H⋯S hydrogen-bonding inter-actions, resulting in a three-dimensional network.

Cyclo-hexyl-ammonium nitrate.

In the title salt, C6H14N(+)·NO3 (-), the cyclo-hexyl ring adopts a chair conformation. The ammonium group occupies an equatorial position and the crystal struture is stabilized by inter-molecular N-H⋯O hydrogen-bonding inter-actions, resulting in a three-dimensional network.

Room-temperature synthesis of zinc oxide nanoparticles in different media and their application in cyanide photodegradation.

Cyanide is an extreme hazard and extensively found in the wastes of refinery, coke plant, and metal plating industries. A simple, fast, cost-effective, room-temperature wet chemical route, based on cyclohexylamine, for synthesizing zinc oxide nanoparticles in aqueous and enthanolic media was established and tested for the photodegradation of cyanide ions. Particles of polyhedra morphology were obtained for zinc oxide, prepared in ethanol (ZnOE), while spherical and some chunky particles were observed for zinc oxide, prepared in water (ZnOW). The morphology was crucial in enhancing the cyanide ion photocatalytic degradation efficiency of ZnOE by a factor of 1.5 in comparison to the efficiency of ZnOW at an equivalent concentration of 0.02 wt.% ZnO. Increasing the concentration wt.% of ZnOE from 0.01 to 0.09 led to an increase in the photocatalytic degradation efficiency from 85% to almost 100% after 180 min and a doubling of the first-order rate constant (k).

γ-Cyclodextrin cuprate sandwich-type complexes.

Three structures, based on γ-cyclodextrin (γ-CD) and metal ions (Cu(2+), Li(+), Na(+), and Rb(+)), have been prepared in aqueous and alkaline media and characterized structurally by single-crystal X-ray diffraction. Their dimeric assemblies adopt cylindrical channels along the c axes in the crystals. Coordinative and hydrogen bonding between the cylinders and the solvent molecules lead to the formation of two-dimensional sheets, with the identity of the alkali-metal ion strongly influencing the precise nature of the solid-state structures. In the case of the Rb(+) complex, coordinative bonding involving the Rb(+) ions leads to the formation of an extended two-dimensional structure. Nonbound solvent molecules can be removed, and gas isotherm analyses confirm the permanent porosity of these new complexes. Carbon dioxide (CO2) adsorption studies show that the extended structure, obtained upon crystallization of the Rb(+)-based sandwich-type dimers, has the highest CO2 sequestration ability of the three γ-CD complexes reported.

Rapid thermally assisted donor-acceptor catenation.

Charged donor-acceptor [2]catenanes containing cyclobis(paraquat-p-phenylene) as the ring component can be synthesised in yields of up to 88% in under one hour by heating two precursors in the presence of macrocyclic polyether templates in N,N-dimethylformamide at 80 °C.

Microwave-assisted synthesis of monodispersed CdTe nanocrystals.

High quality and monodispersed CdTe nanocrystals with tunable emission spectra ranging from 516 nm to 650 nm were synthesized by a highly reproducible microwave method.

A study of laser-induced blue emission with nanosecond decay of silicon nanoparticles synthesized by a chemical etching method.

Silicon nanoparticles (Si NPs), exhibiting a strong visible photoluminescence (PL), have found many applications in optoelectronics devices, biomedical tags and flash memories. Chemical etching is a well-known method for synthesizing orange-luminescent, hydride-capped silicon nanoparticles (H/Si NPs). However, a blueshift in emission wavelength occurs when reducing the particle size to exciton Bohr radius or less. In this paper, we attempted to synthesize and characterize H/Si NPs that emit lower wavelengths at room temperature. We proved that our method succeeded in synthesizing H/Si NPs with emission in the blue region. The wavelength-resolved and time-resolved studies of the PL were executed for H/Si NPs in methanol (MeOH), pyridine (py) and furan, using the 355 nm pulsed radiation from a Nd:YAG laser. In addition, excitation wavelength-dependent and PL studies were executed using the spectrofluorometer with a xenon (Xe) broad band light source. We noticed solvent-dependent PL spectra with sharp peaks near 420 nm and a short lifetime less than 100 ns. The morphology and particle size were investigated by high resolution transmission electron microscope (HRTEM). Particles as small as one nanometer were observed in MeOH and py suspensions while two-nanometer particles were observed in the furan suspension.