MHD Heat and Mass Transfer Steady Flow of a Convective Fluid Through a Porous Plate in The Presence of Diffusion Thermo and Aligned Magnetic Field

In the presence of a diffusion thermal and coupled magnet field effect, this manuscript seeks continuous free convective motion by a viscous, incompressible fluid that conducts electrically past a sloping platform via a porous medium. The free flow speed may be compatible with the exponentially tiny disrupting law. Two-term harmonic and non-harmonic functions solve dimensional-less control equations analytically. Detailed graphs are used to determine the budgets for tempo, temperature, and concentration for various limit calculations. Also, the numbers of Nusselt and Sherwood are given and evaluated with the graphs. Its sketches illustrate that the velocity profiles get reduced by the increase of aligned magnetic field parameter (α) and inclined angle parameter (ξ). Temperature profile is accelerated by rising heat absorption, Dufour number and concentration distribution is decelerated by enhancing the chemical reaction and Schmidt number. Heat and mass transfer frequently occurs in chemically processed industries, distribution of temperature and moisture over agricultural fields, dispersion of fog and environment pollution and polymer production. Free convection flow of coupled heat and mass transfer occurs due to the temperature and concentration differences in the fluid as a result of driving forces. For example, in atmospheric flows, thermal convection resulting from heating of the earth by sunlight is affected differences in water vapour concentration.

Evaluation of convective boundary layer height estimates using radars operating at different frequency bands

Knowledge of the atmospheric boundary layer state and evolution is important for understanding air pollution and low-level cloud development, among other things. There are a number of instruments and methods that are currently used to estimate boundary layer height (BLH). However, no single instrument is capable of providing BLH measurements in all weather conditions. We proposed a method to derive a daytime convective BLH using clear air echoes in radar observations and investigated the consistency of these retrievals between different radar frequencies. We utilized data from three vertically pointing radars that are available at the SMEAR II station in Finland, i.e. the C band (5 GHz), Ka band (35 GHz) and W band (94 GHz). The Ka- or W-band cloud radars are an integral part of cloud profiling stations of pan-European Aerosol, Clouds and Trace Gases Research Infrastructure (ACTRIS). Our method will be utilized at ACTRIS stations to serve as an additional estimate of the BLH during summer months. During this period, insects and Bragg scatter are often responsible for clear air echoes recorded by weather and cloud radars. To retrieve a BLH, we suggested a mechanism to separate passive and independently flying insects that works for all analysed frequency bands. At the lower frequency (the C band) insect scattering has been separated from Bragg scattering using a combination of the radar reflectivity factor and linear depolarization ratio. Retrieved values of the BLH from all radars are in a good agreement when compared to the BLH obtained with the co-located HALO Doppler lidar and ERA5 reanalysis data set. Our method showed some underestimation of the BLH after nighttime heavy precipitation yet demonstrated a potential to serve as a reliable method to obtain a BLH during clear-sky days. Additionally, the entrainment zone was observed by the C-band radar above the CBL in the form of a Bragg scatter layer. Aircraft observations of vertical profiles of potential temperature and water vapour concentration, collected in the vicinity of the radar, demonstrated some agreement with the Bragg scatter layer.

Mechanical–Chemical Coupling Effects on an Environmental Barrier Coating System under High-Temperature Water Vapour Conditions

The degradation mechanisms for environmental barrier coatings (EBCs) under high-temperature water vapour conditions are vital for the service of aero-engine blades. This study proposes a theoretical model of high-temperature water vapour corrosion coupled with deformation, mass diffusion and chemical reaction based on the continuum thermodynamics and the actual water vapour corrosion mechanisms of an EBC system. The theoretical model is suitable for solving the stress and strain fields, water vapour concentration distribution and coating corrosion degree of an EBC system during the water vapour corrosion process. The results show that the thickness of the corrosion zone on the top of the EBC system depended on water vapour diffusion, which had the greatest influence on the corrosion process. The top corroded area of the rare-earth silicate EBC system was significantly evident, and there was a clear dividing line between the un-corroded and corroded regions.

Effect of moisture condensation on vapour transmission through porous membranes

Porous membranes find natural application in various fields and industries. Water condensation on membranes can block pores, reduce vapour transmissibility, and diminish the porous membranes' performance. This research investigates the rate of water vapour transmission through microporous nylon and nanofibrous Gore-Tex membranes. Testing consisted of placing the membrane at the intersection of two chambers with varied initial humidity conditions. One compartment is initially set to a high ([Formula: see text]water vapour concentration and the other low ([Formula: see text], with changes in humidity recorded as a function of time. The impact of pore blockage was explored by pre-wetting the membranes with water or interposing glycerine onto the membrane pores before testing. Pore blockage was measured using image analysis for the nylon membrane. The mass flow rate of water vapour ( ṁv) diffusing through a porous membrane is proportional to both its area (A) and the difference in vapour concentration across its two faces ([Formula: see text], such that [Formula: see text] where K is defined as the moisture diffusion coefficient. Correlations are presented for the variation of K as a function of [Formula: see text]. Liquid contamination on the porous membrane has been shown to reduce the moisture diffusion rate through the membrane due to pore blockage and the subsequent reduced open area available for vapour diffusion. Water evaporation from the membrane's surface was observed to add to the mass of vapour diffusing through the membrane. A model was developed to predict the effect of membrane wetting on vapour diffusion and showed good agreement with experimental data.

Characterization of the time evolution of the PBL structure and dry-layers based on the us of Raman Lidar measurements collected during HYMEX-SOP1

<p>The exchange processes between the Earth and the atmosphere play a crucial role in the development of the Planetary Boundary Layer (PBL). Different remote sensing techniques can provide PBL measurement with different spatial and temporal resolutions. Vertical profiles of atmospheric thermodynamic variables, i.e.  temperature and humidity, or wind speed, clouds and aerosols can be used as proxy to retrieve PBL height from active and passive remote sensing instruments. The University of BASILicata ground-based Raman Lidar system (BASIL) was deployed in the North-Western Mediterranean basin in the Cévennes-Vivarais site (Candillargues, Southern France, Lat: 43°37' N, Long: 4° 4' E, Elev: 1 m) and operated between 5 September and 5 November 2012, collecting more than 600 hours of measurements, distributed over 51 days and 19 intensive observation periods (IOPs). BASIL is capable to provide high-resolution and accurate measurements of atmospheric temperature and water vapour, both in daytime and night-time, based on the application of the rotational and vibrational Raman lidar techniques in the UV. This measurement capability makes BASIL a key instrument for the characterization of the water vapour concentration. BASIL makes use of a Nd:YAG laser source capable of emitting pulses at 355, 532 and 1064 nm, with a single pulse energy at 355nm of 500 mJ [1] .In the presented research effort, water vapour concentration was  computed and used to determine the PBL height. [2]. A dynamic index  included in the European Centre for Medium-range Weather Forecasts (ECMWF) ERA5 atmospheric reanalysis (CAPE, Friction velocity, etc.) is also considered and compared with BASIL resutls. ERA5 provides hourly data on regular latitude-longitude grids at 0.25° x 0.25° resolution at 37 pressure levels [3]. ERA5 is publicly available through the Copernicus Climate Data Store (CDS, https://cds.climate.copernicus.eu).  In order to properly carry out the comparison, the nearest ERA5 grid point to the lidar site has been considered assuming the representativeness uncertainty due to the use of the nearest grid-point comparable with other methods (e.g. kriging, bilinear interpolation, etc.). More results from this  measurement  effort will  be reported and discussed at the Conference.</p><p><strong>Reference</strong></p><p>[1] Di Girolamo, Paolo, De Rosa, Benedetto, Flamant, Cyrille, Summa, Donato, Bousquet, Olivier, Chazette, Patrick, Totems, Julien, Cacciani, Marco. Water vapor mixing ratio and temperature inter-comparison results in the framework of the Hydrological Cycle in the Mediterranean Experiment—Special Observation Period 1. BULLETIN OF ATMOSPHERIC SCIENCE AND TECHNOLOGY, ISSN: 2662-1495, doi: 10.1007/s42865-020-00008-3</p><p>[2] D. Summa, P. Di Girolamo, D. Stelitano, and M. Cacciani. Characterization of the planetary boundary layer height and structure by Raman lidar: comparison of different approaches  Atmos. Meas. Tech., 6, 3515–3525, 2013 www.atmos-meas-tech.net/6/3515/2013/doi:10.5194/amt-6-3515-2013</p><p>[3] Hersbach et al. The ERA5 global reanalysis Hans  https://doi.org/10.1002/qj.3803[3]</p>

Laboratory evaluation of water vapour concentration dependence of commercial water vapour isotope cavity ring-down spectrometers for continuous onsite atmospheric measurements in the Amazon rainforest

<p>Commercially available laser-based spectrometers permit continuous field measurements of water vapour (H<sub>2</sub>O) stable isotope compositions, yet continuous observations in the Amazon, a region that significantly influences atmospheric hydrological cycles on regional to global scales, are largely missing. In order to achieve accurate on-site observations in such conditions, these instruments will require regular on-site calibration, including for H<sub>2</sub>O concentration dependence ([H<sub>2</sub>O]-dependence) of isotopic accuracy.</p><p>With the aim of conducting accurate continuous δ<sup>18</sup>O and δ<sup>2</sup>H on-site observation in the Amazon rainforest, we conducted a laboratory experiment to investigate the performance and determine the optimal [H<sub>2</sub>O]-dependence calibration strategy for two commercial cavity-ring down (CRDS) analysers (L1102i and L2130i models, Picarro, Inc., USA), coupled to our custom-built automated calibration unit. We particularly focused on the rarely investigated performance of the instruments at atmospheric H<sub>2</sub>O contents above 35,000 ppm, a value regularly reached at our site.</p><p>The later analyser model (L2130i) had better precision and accuracy of δ<sup>18</sup>O and δ<sup>2</sup>H measurements with a less pronounced [H<sub>2</sub>O]-dependence compared to the older L1102i. The [H<sub>2</sub>O]-dependence calibration uncertainties did not significantly change with calibration intervals from 28 h up to 196 h, suggesting that one [H<sub>2</sub>O]-dependence calibration per week for the L2130i and L1102i analysers is enough. This study shows that with both CRDS analysers, correctly calibrated, we should be able to discriminate natural diel, seasonal and interannual signals of stable water vapour isotopes in a tropical rainforest environment.</p><p> </p>

Characterizing water vapour concentration dependence of commercial cavity ring-down spectrometers for continuous on-site atmospheric water vapour isotope measurements in the tropics

The recent development and improvement of commercial laser-based spectrometers have expanded in situ continuous observations of water vapour (H2O) stable isotope compositions (e.g. δ18O and δ2H) in a variety of sites worldwide. However, we still lack continuous observations in the Amazon, a region that significantly influences atmospheric and hydrological cycles on local to global scales. In order to achieve accurate on-site observations, commercial water isotope analysers require regular in situ calibration, which includes the correction of H2O concentration dependence ([H2O] dependence) of isotopic measurements. Past studies have assessed the [H2O] dependence for air with H2O concentrations of up to 35 000 ppm, a value that is frequently surpassed in tropical rainforest settings like the central Amazon where we plan continuous observations. Here we investigated the performance of two commercial analysers (L1102i and L2130i models, Picarro, Inc., USA) for measuring δ18O and δ2H in atmospheric moisture at four different H2O levels from 21 500 to 41 000 ppm. These H2O levels were created by a custom-built calibration unit designed for regular in situ calibration. Measurements on the newer analyser model (L2130i) had better precision for δ18O and δ2H and demonstrated less influence of H2O concentration on the measurement accuracy at each concentration level compared to the older L1102i. Based on our findings, we identified the most appropriate calibration strategy for [H2O] dependence, adapted to our calibration system. The best strategy required conducting a two-point calibration with four different H2O concentration levels, carried out at the beginning and end of the calibration interval. The smallest uncertainties in calibrating [H2O] dependence of isotopic accuracy of the two analysers were achieved using a linear surface fitting method and a 28 h calibration interval, except for the δ18O accuracy of the L1102i analyser for which the cubic fitting method gave the best results. The uncertainties in [H2O] dependence calibration did not show any significant difference using calibration intervals from 28 up to 196 h; this suggested that one [H2O] dependence calibration per week for the L2130i and L1102i analysers is sufficient. This study shows that the cavity ring-down spectroscopy (CRDS) analysers, appropriately calibrated for [H2O] dependence, allow the detection of natural signals of stable water vapour isotopes at very high humidity levels, which has promising implications for water cycle studies in areas like the central Amazon rainforest and other tropical regions.