Doped Ceria Catalysts for NOx Storage and Reduction

The new Euro 7 protocol, proposed by the Commission on 26th October 2022, concerning emissions of leanburn engines, presents a need for further optimisation of existing after-treatment technologies. It reveals a 35% reduction to the NOx emission limit for cars and vans, compared to Euro 6 . A well-known technology employed to reduce NOx to clean emissions in light-duty vehicles is the Lean NOx Trap (LNT). LNTs employ catalysts consisting of PGMs supported on ceria (CeO2) or other mixed oxides. Ceria’s redox property makes it an attractive selection, as well as its ability to store NOx at low temp (<300 ̊C), especially when Pt is present. Storage properties of ceria can be further enhanced by doping. Dopants reportedly allow ceria to function better at low temperature (<300 ̊C), and to reduce the PGM loading required to achieve the same conversion efficiencies. The RE metals Sm, Pr and Nd have been employed as dopants on CeO2 for LNT applications to increase surface oxygen content, oxygen vacancies, defect densities, and cause changes to the Pt-ceria interaction. These structural changes can allow for higher NSC during lean operation and enhanced activation during rich purge. Sm, Pr and Nd doped catalysts (10 wt.%) were synthesised on a range of ceria based catalysts with different Pt loadings (0-1 wt.%). Morphological changes observed through dopant addition has been investigated and related to catalytic performance increases.

Coordination Variability after Hip Replacement Surgery: A Case Report

Patients with unilateral hip replacement surgery have an increased risk for additional joint replacement surgeries in the contralateral limb. Reduced coordination variability (Cvar) is associated with orthopedic disorders. Differences in joint Cvar after hip replacement surgery may provide information regarding the progression to a healthier state. The purpose of this study was to examine differences in surgical and contralateral limb knee and hip Cvar before and after surgery. A male participant completed gait analyses prior to total hip arthroplasty, three weeks following surgery (post-op) and ten months after surgery. He walked at a preferred speed while three-dimensional kinematic and kinetic data were recorded. A modified vector coding technique was used to determine the bilateral Cvar throughout stance for thigh-leg and pelvis-thigh flexion/extension and internal/external rotation coordination. Cvar was averaged for the stance phase of gait at each visit. Effect Size (ES) was calculated to determine clinically significant differences in variability both between the surgical and contralateral limbs and for each visit (Tables 1 and 2). In the surgical limb, variability was similar at all visits for pelvis-thigh and thigh-shank flexion/extension and internal/external rotation (ES\u3c0.5). Differences in (Cvar) between the surgical and contralateral limbs diminished with time. While Cvar in the surgical limb did not change, Cvar in the contralateral limb decreased over time. This may indicate a decline in health and an increased risk for orthopedic disorders in the contralateral limb after hip replacement surgery

SYMPOSIUM ON RECENT DEVELOPMENTS IN DATA ANALYSIS

The purpose of this symposium is to present recent developments in biomechanical data analyses in two areas. First, current methods used in a dynamical systems approach will be described. Second, two statistical approaches, Principal Components Analysis and Functional Data Analysis, will be presented. The emphasis in this symposium will be on how to use each of these recent analysis techniques

Out of the boxes, out of the silos: The need of interdisciplinary collaboration to reduce poor-quality medical products in the supply chain

In this paper, we argue that understanding and addressing the problem of poor-quality medical products requires a more interdisciplinary approach than has been evident to date. While prospective studies based on rigorous standardized methodologies are the gold standard for measuring the prevalence of poor-quality medical products and understanding their distribution nationally and internationally, they should be complemented by social science research to unpack the complex set of social, economic, and governance factors that underlie these patterns. In the following sections, we discuss specific examples of prospective quality surveys and of social science studies, highlighting the value of cross-sector partnerships in driving high-quality, policy-relevant research in this area

The effect of the bend on technique and performance during maximal effort sprinting

This study investigated changes in performance and technique that occur during maximal effort bend sprinting compared to straight-line sprinting under typical outdoor track conditions. Utilising a repeated measures design, three-dimensional video analysis was conducted on seven male sprinters in both conditions (bend radius: 37.72 m). Mean race velocity decreased from 9.86 m/s to 9.39 m/s for the left step (p = 0.008) and from 9.80 m/s to 9.33 m/s for the right step (p = 0.004) on the bend compared to the straight, a 4.7% decrease for both steps. This was due mainly to a 0.11 Hz (p = 0.022) decrease in step frequency for the left step and a 0.10 m (p = 0.005) reduction in race step length for the right step. The left hip was 4.0° (p = 0.049) more adducted at touchdown on the bend than the straight. Furthermore, the bend elicited significant differences between left and right steps in a number of variables including ground contact time, touchdown distance and hip flexion/extension and abduction/adduction angles. The results indicate that the roles of the left and right steps may be functionally different during bend sprinting. This specificity should be considered when designing training programmes

Gating-by-tilt of mechanosensitive membrane channels

We propose an alternative mechanism for the gating of biological membrane channels in response to membrane tension that involves a change in the slope of the membrane near the channel. Under biological membrane tensions we show that the energy difference between the closed (tilted) and open (untilted) states can far exceed kBT and is comparable to what is available under simple ilational gating. Recent experiments demonstrate that membrane leaflet asymmetries (spontaneous curvature) can strong effect the gating of some channels. Such a phenomenon would be more easy to explain under gating-by-tilt, given its novel intrinsic sensitivity to such asymmetry.Comment: 10 pages, 2 figure

Multi-parameter models of innovation diffusion on complex networks

A model, applicable to a range of innovation diffusion applications with a strong peer to peer component, is developed and studied, along with methods for its investigation and analysis. A particular application is to individual households deciding whether to install an energy efficiency measure in their home. The model represents these individuals as nodes on a network, each with a variable representing their current state of adoption of the innovation. The motivation to adopt is composed of three terms, representing personal preference, an average of each individual's network neighbours' states and a system average, which is a measure of the current social trend. The adoption state of a node changes if a weighted linear combination of these factors exceeds some threshold. Numerical simulations have been carried out, computing the average uptake after a sufficient number of time-steps over many realisations at a range of model parameter values, on various network topologies, including random (Erdos-Renyi), small world (Watts-Strogatz) and (Newman's) highly clustered, community-based networks. An analytical and probabilistic approach has been developed to account for the observed behaviour, which explains the results of the numerical calculations

Managing suicidal ideation in a breast cancer cohort seeking reconstructive surgery

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/135255/1/pon4017_am.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/135255/2/pon4017.pd

A Systems Engineering Approach to Modeling and Analysis of Chronic Obstructive Pulmonary Disease (COPD)

Chronic Obstructive Pulmonary Disease (COPD) is a progressive lung disease characterized by airflow limitation. This study develops a systems engineering framework for representing important mechanistic details of COPD in a model of the cardio-respiratory system. In this model, we present the cardio-respiratory system as an integrated biological control system responsible for regulating breathing. Four engineering control system components are considered: sensor, controller, actuator, and the process itself. Knowledge of human anatomy and physiology is used to develop appropriate mechanistic mathematical models for each component. Following a systematic analysis of the computational model, we identify three physiological parameters associated with reproducing clinical manifestations of COPD - changes in the forced expiratory volume (FEV), lung volumes, and pulmonary hypertension. We quantify the changes in these parameters (airway resistance, lung elastance, and pulmonary resistance) as the ones that result in a systemic response that is diagnostic of COPD. A multivariate analysis reveals that the changes in airway resistance have a broad impact on the human cardio-respiratory system, and that the pulmonary circuit is stressed beyond normal under hypoxic environments in most COPD patients.Comment: 25 pages, 15 figure

Activation of native TRPC1/C5/C6 channels by endothelin-1 is mediated by both PIP3 and PIP2 in rabbit coronary artery myocytes

We investigate activation mechanisms of native TRPC1/C5/C6 channels (termed TRPC1 channels) by stimulation of endothelin-1 (ET-1) receptor subtypes in freshly dispersed rabbit coronary artery myocytes using single channel recording and immunoprecipitation techniques. ET-1 evoked non-selective cation channel currents with a unitary conductance of 2.6 pS which were not inhibited by either ET(A) or ET(B) receptor antagonists, respectively BQ-123 and BQ788, when administered separately. However, in the presence of both antagonists, ET-1-evoked channel activity was abolished indicating that both ET(A) and ET(B) receptor stimulation activate this conductance. Stimulation of both ET(A) and ET(B) receptors evoked channel activity which was inhibited by the protein kinase C (PKC) inhibitor chelerythrine and by anti-TRPC1 antibodies indicating that activation of both receptor subtypes causes TRPC1 channel activation by a PKC-dependent mechanism. ET(A) receptor-mediated TRPC1 channel activity was selectively inhibited by phosphoinositol-3-kinase (PI-3-kinase) inhibitors wortmannin (50 nm) and PI-828 and by antibodies raised against phosphoinositol-3,4,5-trisphosphate (PIP(3)), the product of PI-3-kinase-mediated phosphorylation of phosphatidylinositol 4,5-bisphosphate (PIP(2)). Moreover, exogenous application of diC8-PIP(3) stimulated PKC-dependent TRPC1 channel activity. These results indicate that stimulation of ET(A) receptors evokes PKC-dependent TRPC1 channel activity through activation of PI-3-kinase and generation of PIP(3). In contrast, ET(B) receptor-mediated TRPC1 channel activity was inhibited by the PI-phospholipase C (PI-PLC) inhibitor U73122. 1-Oleoyl-2-acetyl-sn-glycerol (OAG), an analogue of diacylglycerol (DAG), which is a product of PI-PLC, also activated PKC-dependent TRPC1 channel activity. OAG-induced TRPC1 channel activity was inhibited by anti-phosphoinositol-4,5-bisphosphate (PIP(2)) antibodies and high concentrations of wortmannin (20 μm) which depleted tissue PIP(2) levels. In addition exogenous application of diC8-PIP(2) activated PKC-dependent TRPC1 channel activity. These data indicate that stimulation of ET(B) receptors evokes PKC-dependent TRPC1 activity through PI-PLC-mediated generation of DAG and requires a permissive role of PIP(2). In conclusion, we provide the first evidence that stimulation of ET(A) and ET(B) receptors activate native PKC-dependent TRPC1 channels through two distinct phospholipids pathways involving a novel action of PIP(3), in addition to PIP(2), in rabbit coronary artery myocytes