Butane Dry Reforming Catalyzed by Cobalt Oxide Supported on Ti2AlC MAX Phase

MAX (M(n+1)AX(n)) phases are layered carbides or nitrides with a high thermal and mechanical bulk stability. Recently, it was shown that their surface structure can be modified to form a thin non-stoichiometric oxide layer, which can catalyze the oxidative dehydrogenation of butane. Here, the use of a Ti2AlC MAX phase as a support for cobalt oxide was explored for the dry reforming of butane with CO2, comparing this new catalyst to more traditional materials. The catalyst was active and selective to synthesis gas. Although the surface structure changed during the reaction, the activity remained stable. Under the same conditions, a titania-supported cobalt oxide catalyst gave low activity and stability due to the agglomeration of cobalt oxide particles. The Co3O4/Al(2)O(3)catalyst was active, but the acidic surface led to a faster deactivation. The less acidic surface of the Ti2AlC was better at inhibiting coke formation. Thanks to their thermal stability and acid-base properties, MAX phases are promising supports for CO(2)conversion reactions

Molybdenum Oxide Supported on Ti3AlC2 is an Active Reverse Water−Gas Shift Catalyst

MAX phases are layered ternary carbides or nitrides that are attractive for catalysis applications due to their unusual set of properties. They show high thermal stability like ceramics, but they are also tough, ductile, and good conductors of heat and electricity like metals. Here, we study the potential of the Ti(3)AlC(2 )MAX phase as a support for molybdenum oxide for the reverse water-gas shift (RWGS) reaction, comparing this new catalyst to more traditional materials. The catalyst showed higher turnover frequency values than MoO3/TiO2 and MoO3/Al2O3 catalysts, due to the outstanding electronic properties of the Ti3AlC2 support. We observed a charge transfer effect from the electronically rich Ti3AlC2 MAX phase to the catalyst surface, which in turn enhances the reducibility of MoO3 species during reaction. The redox properties of the MoO3/Ti3AlC2 catalyst improve its RWGS intrinsic activity compared to TiO2- and Al2O3-based catalysts

Typing of Salmonella Typhi strains isolated from Egypt by RAPD PCR

PCR-based fingerprinting using random amplified polymorphic DNA (RAPD) has been used widely for genome identification. In this study, 13 Salmonella Typhi strains were isolated from typhoid patients from Aswan, Cairo, Fayoum, and Monofya Governorates of Egypt. The isolates, along with three reference strains, i.e., O901, H901, and Ty2 were subjected to whole genome typing by RAPD PCR. Three RAPD-PCR 10-mer primers generated a total of 85 RAPD bands (81 polymorphic bands), 12 distinct PCR profiles, and proved to be useful for discriminating the isolates and strains studied. Interestingly, the B1 and C1 PCR profile were found only in Cairo and Monofya, respectively; and some PCR types appeared only in certain Governorates of Egypt. By combining the profiles obtained with the primer trio used in this study, an excellent discrimination index (D) of 0.942 was reached. Pairwise comparisons of Jaccard’s similarity coefficients calculated among the 12 PCR types identified three major clusters; i.e., O901 branch and Ty2 and H901 sub-branches. Principal component analysis adequately resolved each of these three major clusters. Three principal components accounted for about 72% of the variation, with the first two components accounting for about 62% of the total variance among the genotypes studied. Biclustering improved the display of groups of RAPD amplicons (markers) that cluster similarly across the genomes and could delineate features pertaining to genome structure. In conclusion, RAPD PCR provided a fast method with high potentials in surveillance and epidemiological investigations of Salmonella Typhi infections

Evaluation of appendicitis risk prediction models in adults with suspected appendicitis

Background Appendicitis is the most common general surgical emergency worldwide, but its diagnosis remains challenging. The aim of this study was to determine whether existing risk prediction models can reliably identify patients presenting to hospital in the UK with acute right iliac fossa (RIF) pain who are at low risk of appendicitis. Methods A systematic search was completed to identify all existing appendicitis risk prediction models. Models were validated using UK data from an international prospective cohort study that captured consecutive patients aged 16–45 years presenting to hospital with acute RIF in March to June 2017. The main outcome was best achievable model specificity (proportion of patients who did not have appendicitis correctly classified as low risk) whilst maintaining a failure rate below 5 per cent (proportion of patients identified as low risk who actually had appendicitis). Results Some 5345 patients across 154 UK hospitals were identified, of which two‐thirds (3613 of 5345, 67·6 per cent) were women. Women were more than twice as likely to undergo surgery with removal of a histologically normal appendix (272 of 964, 28·2 per cent) than men (120 of 993, 12·1 per cent) (relative risk 2·33, 95 per cent c.i. 1·92 to 2·84; P < 0·001). Of 15 validated risk prediction models, the Adult Appendicitis Score performed best (cut‐off score 8 or less, specificity 63·1 per cent, failure rate 3·7 per cent). The Appendicitis Inflammatory Response Score performed best for men (cut‐off score 2 or less, specificity 24·7 per cent, failure rate 2·4 per cent). Conclusion Women in the UK had a disproportionate risk of admission without surgical intervention and had high rates of normal appendicectomy. Risk prediction models to support shared decision‐making by identifying adults in the UK at low risk of appendicitis were identified

Highly active and stable Co (Co3O4)_Sm2O3 nano-crystallites derived from Sm2Co7 and SmCo5 intermetallic compounds in NH3 synthesis and CO2 conversion

Intermetallic compounds (IMCs) are interesting materials in the field of heterogeneous catalysis due to their ordered structure and tunable electronic properties. These IMCs can act as precursor to synthesize metal/metal oxide composite catalysts that are more active than just the starting IMCs. In this work, Sm2Co7 and SmCo5 IMCs were used as precursors to prepare highly active and stable Co_SmO, Co_Sm2O3 and Co3O4_Sm2O3 catalysts via controlled modification. Transmission electron microscopy (TEM) demonstrated that Co and Sm2O3 Nano crystallites were formed after the modification of the IMC. IMCs derived Co_SmO and Co_Sm2O3 were stable and active in NH3 synthesis with very low activation energy of 55 and 77 kJ mol−1 respectively. The structural, morphological and surface characterization revealed that a strong metal support interaction existed between Co and Sm2O3 (electronic effect) along with the presence of surface steps and edges of Co nano crystallites (structural effect) that activate the N2 at low temperature (360 °C). Similarly, Co3O4_Sm2O3 derived from the IMC were found to exhibit high CO2 and butane conversion in butane dry reforming at low temperature (550 °C) with excellent stability. The study revealed that the presence of Co3O4 and Sm2O3 active sites in close proximity (geometrical effect) promoted the simultaneous adsorption or activation of butane and CO2. The Co_Sm2O3 and Co3O4_Sm2O3 derived from IMCs exhibited superior catalytic performance in both NH3 synthesis and butane dry reforming compared to similar compositional catalyst synthesized by hydrothermal route. These studies pave the way to potential uses of IMCs as precursors to derive composite metal/metal oxide catalysts that are highly stable and active despite their low surface areas

Highly Active and Stable Co (Co3O4)_Sm2O3 Nano-crystallites Derived from Sm2Co7 and SmCo5 Intermetallic Compounds in NH3 Synthesis and CO2 Conversion

Intermetallic compounds (IMCs) are interesting materials in the field of heterogeneous catalysis due to their ordered structure and tunable electronic properties. These IMCs can act as precursor to synthesize metal/metal oxide composite catalysts that are more active than just the starting IMCs. In this work, Sm2Co7 and SmCo5 IMCs were used as precursors to prepare highly active and stable Co_SmO, Co_Sm2O3 and Co3O4_Sm2O3 catalysts via controlled modification. Transmission electron microscopy (TEM) demonstrated that Co and Sm2O3 Nano crystallites were formed after the modification of the starting IMC. IMCs derived Co_SmO and Co_Sm2O3 were stable and active in NH3 synthesis with very low activation energy of 55 and 77 kJ/mol respectively. The structural, morphological and surface characterization revealed that a strong metal support interaction existed between Co and Sm2O3 (electronic effect) along with the presence of surface steps and edges of Co nano crystallites (structural effect) that activated the N2 at low temperature (360 °C). Similarly, Co3O4_Sm2O3 derived from the IMC were found to exhibit high CO2 and butane conversion in butane dry reforming at low temperature (550 °C) with excellent stability. The study revealed that the presence of Co3O4 and Sm2O3 active sites in close proximity (geometrical effect) promoted the simultaneous adsorption or activation of butane and CO2. The Co_Sm2O3 and Co3O4_Sm2O3 derived from IMCs exhibited superior catalytic performance in both NH3 synthesis and butane dry reforming compared to similar compositional catalyst synthesized by hydrothermal route. These studies pave the way to potential uses of IMCs as precursors to derive composite metal/metal oxide catalysts that are highly stable and active despite their low surface areas