Mccormackrobbins7555

Maternal infection (i.e., ascending infection) and the resulting host inflammatory response are risk factors associated with spontaneous preterm birth (PTB), a major pregnancy complication. However, the path of infection and its propagation from the maternal side to the fetal side have been difficult to study due to the lack of appropriate in vitro models and limitations of animal models. A better understanding of the propagation kinetics of infectious agents and development of the host inflammatory response at the feto-maternal (amniochorion-decidua, respectively) interface (FMi) is critical in curtailing host inflammatory responses that can lead to PTB. To model ascending infection and determine inflammatory responses at the FMi, we developed a microfluidic organ-on-chip (OOC) device containing primary cells from the FMi (decidua, chorion, and amnion [mesenchyme and epithelium]) and collagen matrix harvested from primary tissue. The FMi-OOC is composed of four concentric circular cell/collagen chambers desiponse at the FMi indicative of pathologic pathways of PTB. This OOC model provides a novel platform to study physiological and pathological cell status at the FMi, and is expected to have broad utility in the field of obstetrics.C2 separation is of great importance in the petrochemical industry. Traditionally, it is performed by distillation at cryogenic temperatures, which necessitates the consumption of a huge amount of energy to operate the refrigeration system in the production process. In this regard, it is imperative to seek alternative separation methods with high efficiency and low energy cost. Although of recent origin, metal-organic frameworks (MOFs) have already been extensively studied as advanced adsorbents in many applications, and significant progress has been made particularly in gas separation owing to their unprecedented porosity and tunable structures. In this review, we extrapolated three most frequently invoked design strategies for efficient C2 separation hinged upon supramolecular interactions, including molecular sieving, gate opening, and surface engineering. read more Recent progress of MOF materials in C2 separation was highlighted within each of these strategies, and their advantages and limitations are compared and discussed. Accordingly, we provide perspectives on current challenges and future emphases in designing MOF materials for hydrocarbon separation. With our continued efforts in this area, we expect that integrating supramolecular interactions in a single MOF system is a viable approach to achieve a balance between adsorption capacity and selectivity for different hydrocarbon separation scenarios.For the challenge of stabilizing a fullerene-like borospherene, a perfect fullerene-like borospherene B20 with Ih symmetry is stabilized theoretically for the first time by selected 12 η5 (pentahapto)-Mg atoms capped on the 12 B5 pentagons, forming an exohedral metalloborospherene Ih Mg12&B20 molecule. Owing to the pull-push electron transfer relay, the molecule is converted to a spherical electride molecule (Mg2+)12&B2018- + 6e- with multiexcess electrons and high-valent B2018- polyanion with a full-shell electronic configuration, performing the stabilization of the fullerene-like B20 cage. Furthermore, we embed the metal M atom in the B20 cage, forming new endohedral electride molecules (Mg2+)12&(Mn+@B2018-) + (6 + n)e- (M = Li, n = 1 and Mg, n = 2). The embedded atom M increases the excess electron number. Notably, these electride molecules possess two different types of superatomic characteristics, exhibiting the behavior of an electron reservoir. Moreover, a compound (Mg12&B20)2O is designed and obtained, so Mg12&B20 might serve as a nano-building block. In addition, the Mg12&B20 and Mg12&(Mg@B20) electride molecules are efficient external electric field-manipulated nonlinear optical (NLO) switches with high sensitivity and reversibility. The embedding metal atom in the B20 cage can also serve as a new strategy to manipulate NLO switching.Due to the more volatile nature of 210Po in relation to 210Pb, an imbalance of activity concentrations in high temperature combustion processes can be observed, especially in fine particulates (diameter less then 0.1, 0.2 and 0.5 μm). In the atmosphere and in the soil around coal-fired power plants, 210Pb and 210Po concentrations are a combination of activities from natural and anthropogenic sources. In this study only portions of 210Po and 210Pb radionuclides resulting from energy production activities were analyzed. Due to the high mobility of fine particles, a surface area of 172 km × 140 km in central Poland was chosen for simulation. For validation of the modeling approach, three grid versions were applied 1 km, 2 km and 4 km. Simulated results confirmed experimental-computational values of an excess of both radionuclides in the atmosphere in 2017 in the city of Lodz. Different aerosol fractions, seasons and various grids in the selected area were subjected to 36 individual simulations. The 210Po activity concentrations measured in winter and summer 2017 were 42.5 and 8.99 μBq m-3, respectively. Simulated and measured values of artificial 210Po and 210Pb activities are well correlated.Reflection absorption infrared spectroscopy and temperature programmed desorption were used to study the adsorption of acrolein, its partial hydrogenation products, propanal and 2-propenol, and its full hydrogenation product, 1-propanol on the Ag(111) surface. Each molecule adsorbs weakly to the surface and desorbs without reaction at temperatures below 220 K. For acrolein, the out-of plane bending modes are more intense than the C[double bond, length as m-dash]O stretch at all coverages, indicating that the molecular plane is mainly parallel to the surface. The two alcohols, 2-propenol and 1-propanol, have notably higher desorption temperatures than acrolein and display strong hydrogen bonding in the multilayers as revealed by a broadened and redshifted O-H stretch. For 1-propanol, annealing the surface to 180 K disrupts the hydrogen-bonding to produce unusally narrow peaks, including one at 1015 cm-1 with a full width at half maximum of 1.1 cm-1. This suggests that 1-propanol forms a highly orderded monolayer and adsorbs as a single conformer.