Reduction of acoustic disturbances in the test section of supersonic wind tunnels by laminarizing their nozzle and test section wall boundary layers by means of suction

The feasibility of quiet, suction laminarized, high Reynolds number (Re) supersonic wind tunnel nozzles was studied. According to nozzle wall boundary layer development and stability studies, relatively weak area suction can prevent amplified nozzle wall TS (Tollmien-Schlichting) boundary layer oscillations. Stronger suction is needed in and shortly upstream of the supersonic concave curvature nozzle area to avoid transition due to amplified TG (Taylor-Goertler) vortices. To control TG instability, moderately rapid and slow expansion nozzles require smaller total suction rates than rapid expansion nozzles, at the cost of larger nozzle length Re and increased TS disturbances. Test section mean flow irregularities can be minimized with suction through longitudinal or highly swept slots (swept behind local Mach cone) as well as finely perforated surfaces. Longitudinal slot suction is optimized when the suction-induced crossflow velocity increases linearly with surface distance from the slot attachment line toward the slot (through suitable slot geometry). Suction in supersonic blowdown tunnels may be operated by one or several individual vacuum spheres

Low speed tests of a fixed geometry inlet for a tilt nacelle V/STOL airplane

Test data were obtained with a 1/4 scale cold flow model of the inlet at freestream velocities from 0 to 77 m/s (150 knots) and angles of attack from 45 deg to 120 deg. A large scale model was tested with a high bypass ratio turbofan in the NASA/ARC wind tunnel. A fixed geometry inlet is a viable concept for a tilt nacelle V/STOL application. Comparison of data obtained with the two models indicates that flow separation at high angles of attack and low airflow rates is strongly sensitive to Reynolds number and that the large scale model has a significantly improved range of separation-free operation

Transonic and supersonic test of a Mach 2.65 mixed-compression axisymmetric intake

The test results describe isolated intake performance between Mach 0.95 and the cruise Mach number of 2.65 at angles of incidence from +5 to -5 deg. Maximum total pressure recoveries of over 94 percent with 10 percent distortion were recorded at the compressor face in the Mach range from 2.65 to 2.4. Typical cruise operating recovery was 91 percent with 13 percent distortion, 7 percent bleed, 5 percent corrected flow stability margin, and 2.2 deg angle-of-incidence tolerance without need for control action. In the started range below Mach 2.4, recoveries were 2 percent to 4 percent lower than the recoveries above Mach 2.4, and the distortion increased to approximately 20 percent. At Mach 0.95 the maximum measured capture flow was 99.4 percent of the theoretical choked value. The recovery was 97.1 percent with less than 10 percent distortion

Low speed and angle of attack effects on sonic and near-sonic inlets

Tests of the Quiet, Clean Short-Haul Experimental Engine (QCSEE) were conducted to determine the effects of forward velocity and angle of attack on sonic and near-sonic inlet aerodynamic performance penalties and acoustic suppression characteristics. The tests demonstrate that translating centerbody and radial vane sonic inlets, and QCSEE high throat Mach number inlets, can be designed to operate effectively at forward speed and moderate angle of attack with good performance and noise suppression capability. The test equipment and procedures used in conducting the evaluation are described. Results of the tests are presented in tabular form

The role of the P2X7 receptor on bone loss in a mouse model of inflammation-mediated osteoporosis

In inflammatory autoimmune diseases, bone loss is frequent. In most cases, secondary osteoporosis is caused by treatment with systemic glucocorticoid. However, the pathogenesis behind the bone loss is presumed multifactorial. We aimed to elucidate the role of the P2X7 receptor on bone mineral density (BMD), microarchitecture, and bone strength in a standardized mouse model of inflammation-mediated osteoporosis (IMO). In total 146 mice completed our protocol, 70 wild type (WT) mice and 76 P2X7−/− (knockout, KO). BMD at the femur and spine decreased significantly from baseline to day 20 in the WT IMO mice (p < 0.01). In the WT vehicle, KO vehicle and KO IMO, no significant BMD changes were found. Bone strength showed a lower mid-shaft max strength (p = 0.038) and also a non-significant trend towards lower strength at the femoral neck of the WT IMO group. Trabecular bone volume fraction (BV/TV) and connectivity density (CD) after 20 days were significantly decreased in the WT IMO group (p = 0.001). In contrast, the WT vehicle and KO vehicle, BV/TV and CD did no change at 20 days. Cortical bone revealed no significant microarchitectural changes after 20 days in the WT IMO group, whereas the total cortical area increased significantly in WT vehicle and KO IMO after 20 days (5.2% and 8.8%, respectively). In conclusion, the P2X7 receptor KO mice did not respond to inflammation with loss of BMD whereas the WT mice had a significant loss of BMD, bone strength and trabecular microarchitecture, demonstrating a role for the P2X7 receptor in inflammatory bone loss

Genetic background strongly influences the bone phenotype of P2X7 receptor knockout mice

The purinergic P2X7 receptor is expressed by bone cells and has been shown to be important in both bone formation and bone resorption. In this study we investigated the importance of the genetic background of the mouse strains on which the P2X7 knock-out models were based by comparing bone status of a new BALB/cJ P2X7-/- strain with a previous one based on the C57BL/6 strain. Female four-month-old mice from both strains were DXA scanned on a PIXImus densitometer; femurs were collected for bone strength measurements and serum for bone marker analysis. Bone-related parameters that were altered only slightly in the B6 P2X7-/- became significantly altered in the BALB/cJ P2X7-/- when compared to their wild type littermates. The BALB/cJ P2X7-/- showed reduced levels of serum C-telopeptide fragment (s-CTX), higher bone mineral density, and increased bone strength compared to the wild type littermates. In conclusion, we have shown that the genetic background of P2X7-/- mice strongly influences the bone phenotype of the P2X7-/- mice and that P2X7 has a more significant regulatory role in bone remodeling than found in previous studies

Extracellular ATP released by osteoblasts is a key local inhibitor of bone mineralisation

Previous studies have shown that exogenous ATP (>1µM) prevents bone formation in vitro by blocking mineralisation of the collagenous matrix. This effect is thought to be mediated via both P2 receptor-dependent pathways and a receptor-independent mechanism (hydrolysis of ATP to produce the mineralisation inhibitor pyrophosphate, PPi). Osteoblasts are also known to release ATP constitutively. To determine whether this endogenous ATP might exert significant biological effects, bone-forming primary rat osteoblasts were cultured with 0.5-2.5U/ml apyrase (which sequentially hydrolyses ATP to ADP to AMP + 2Pi). Addition of 0.5U/ml apyrase to osteoblast culture medium degraded extracellular ATP to <1% of control levels within 2 minutes; continuous exposure to apyrase maintained this inhibition for up to 14 days. Apyrase treatment for the first 72 hours of culture caused small decreases (≤25%) in osteoblast number, suggesting a role for endogenous ATP in stimulating cell proliferation. Continuous apyrase treatment for 14 days (≥0.5U/ml) increased mineralisation of bone nodules by up to 3-fold. Increases in bone mineralisation were also seen when osteoblasts were cultured with the ATP release inhibitors, NEM and brefeldin A, as well as with P2X1 and P2X7 receptor antagonists. Apyrase decreased alkaline phosphatase (TNAP) activity by up to 60%, whilst increasing the activity of the PPi-generating ecto-nucleotide pyrophosphatase/phosphodiesterases (NPPs) up to 2.7-fold. Both collagen production and adipocyte formation were unaffected. These data suggest that nucleotides released by osteoblasts in bone could act locally, via multiple mechanisms, to limit mineralisation

Ecological risk assessment framework for microplastics in agricultural soils amended with biosolids

This study conceptualizes a framework for ecological risk assessment of microplastics (MPs) in agricultural soils amended with biosolids. MPs in biosolids pose risks to soil biota, affecting soil health. The study highlights the complexity of assessing MP risks, considering not only MPs abundance, but also properties such as size, shape, and type. To develop this framework for ecological risk assessment of MPs in agricultural soils amended with biosolids, a literature review was conducted to systematically assess effects of different MPs properties on soil organisms. Earthworms, springtails, and the microbiome were considered as receptors. The study highlights the importance of understanding MPs fate in soil, since effects on soil biota can be time dependent. Furthermore, results show that organisms respond differently to similar MPs properties, increasing the complexity of assessing MPs risks in terrestrial ecosystems. This complexity also relates to MPs effects on soil properties, and indirect effects on soil biota. Further research is needed to address knowledge gaps for effects of specific MPs properties to better assess and manage ecological risks in agricultural systems