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Summary: Partial oxidation of methane was studied over new Ni nanocatalysts prepared from Ni‐impregnated γ‐AlOOH, which were compared with their counterparts derived from impregnated γ‐Al2O3 and α‐Al2O3. The prepared catalysts were characterized by powder X‐ray diffraction (XRD), N2‐sorption, H2‐temperatue programmed reduction, scanning electron microscopy, transmission electron microscopy, thermal gravimetric analysis, CO2‐ and NH3‐temperature‐programmed desorption, Raman spectroscopy, CO chemisorption, and diffuse reflectance infrared Fourier transform spectroscopy of adsorbed CO. Employing γ‐AlOOH as the support precursor resulted in significantly improved textural properties and catalytic activity. The structure of the support precursor and its surface properties showed a strong influence on the type of Ni active species and their interactions with the support. γ‐AlOOH‐derived catalysts showed NiO as the dominant Ni species when calcined at 500°C to 650°C, while NiAl2O4 became the sole phase at higher temperatures. On the other hand, mixtures of NiO and NiAl2O4 formed over γ‐Al2O3, calcined before impregnation, regardless of the precalcination temperature. All γ‐AlOOH‐derived catalysts showed higher specific surface areas compared to their counterparts derived from impregnated γ‐Al2O3. Upon calcination at moderate temperatures, γ‐AlOOH‐derived catalysts also showed modified textural and morphological properties of the Ni active particles, including higher Ni dispersion, larger metal surface area, and smaller Ni crystallites. The support precursor and the pretreatment conditions showed a strong influence on the catalytic performance, which was referred to their significant effect on the type of the Ni species and interactions with the support. All catalysts showed higher catalytic activity than the α‐Al2O3‐derived catalyst, with CH4 conversion between 86% and 88.5% at 700°C. While γ‐AlOOH‐ and γ‐Al2O3‐derived catalysts calcined at 650°C showed a stable CH4 conversion around 88%, and higher syngas selectivity than the other catalysts, Ni/γ‐AlOOH‐650 showed the highest selectivity to syngas, with a H2/CO ratio very close to 2.0. The improved Ni dispersion and the enhanced syngas selectivity obtained in the preset work demonstrate that using γ‐AlOOH as a support precursor holds a great promise for the development of a new route for more efficient Ni catalysts compared with the widely studied γ‐Al2O3 and α‐Al2O3 support precursors. [ABSTRACT FROM AUTHOR]

Vitamin D deficiency is being recognized as a global issue and has been implicated in many health issues. Hence, there is an increased interest in developing sensitive, reproducible, and non-invasive assays to measure Vitamin D levels. This study aimed to apply a sensitive liquid chromatography-mass spectrometric assay to hair samples to develop and validate a clinical assay to provide a quarterly average level of vitamin D in one test. Hair samples were collected from 70 male university students/young adults and pulverized/sonicated in methanol/water for 2 h to extract Vitamin D metabolites. A sensitive liquid chromatographic-mass spectrometric assay was employed to quantitate vitamin D and metabolites. Of the eight Vitamin D and metabolites screened, only the primary, clinically significant form of vitamin D (25OHD3) was detected and quantified in hair samples in the range of 17–1541 pg/mg. One-third of the hair samples (21 out of 70) had Vitamin D levels below the LLOD of the assay (10 pg/mg). The mean and standard deviation values for hair (25OHD3) were 276.7 ± 329.9, respectively. This pilot study reveals the potential of the vitamin D hair test in clinical assays as a complementary test to a vitamin D blood test, which would provide a quarterly average. [ABSTRACT FROM AUTHOR]