Μm Diameter Particles Research Articles

Developing and testing low-cost air cleaners for safer spaces during wildfires

Air cleaning reduces indoor exposure to fine particulate matter (PM2.5) during wildfire smoke events. However, resource and cost constraints may limit access to air cleaning during such an event, as both commercial devices and the higher-rated MERV filters that do-it-yourself (DIY) assemblies typically rely upon tend to be expensive and in short supply. With these constraints in mind, we developed and evaluated several configurations of a novel, DIY air cleaner that uses common household fabrics as filtration media. Clean air delivery rates (CADRs) of the devices were experimentally evaluated in two ways: first, with independent measurements of flowrates and single pass removal efficiencies, and second, via pull-down testing in a large chamber. With two layers of cotton batting fabric and a flowrate-increasing cardboard shroud attached, the device achieved particulate matter CADRs of 162, 134, and 206 m3/h in 0.02–0.3, 0.3–1, and 1–2.5 µm particle diameter bins, respectively, during chamber testing. Results indicate that these simple, inexpensive, fabric configurations can meaningfully reduce PM2.5 levels in smaller zones of a home, and thus represent a viable option for improving indoor air quality during rapid-onset air pollution events, such as wildfires.

Detonation Soot: A New Class of Ice Nucleating Particle

AbstractTemperatures and pressures from high explosive detonations far exceed atmospheric conditions in typical combustion reactions, and consequently, detonation soot forms with physiochemical properties distinct from soot formed by combustion. In this study, samples of detonation soot from two high explosives, PBX 9502 and Composition B‐3, were analyzed. Ice nucleation experiments on soot collected after controlled detonations were conducted in the laboratory to probe immersion and contact mode freezing. Samples nucleated ice at temperatures warmer than commercially available nanodiamonds, which has a mean nucleation temperature of −20.7°C. Ice nucleation rate coefficients increase rapidly by two to three orders of magnitude below −20°C for every sample. Size‐selected 137 μm diameter particles produced during detonation in an ambient air atmosphere yield bimodal distributions of freezing temperature with primary and secondary nucleation modes centered at −20°C and −13°C, respectively. The presence of a secondary mode allows for enhanced ice nucleation rate coefficients (one to two orders of magnitude greater than samples without a secondary mode) at temperatures outside the influence of the primary mode (>−17°C). Given the observed onset nucleation temperatures of −9.2°C, our results imply that detonation soot of the type studied here would only need to reach an altitude of approximately 4 km to facilitate ice formation.

Selective leaching behavior of Nd from spent NdFeB magnets treated with combination of selective oxidation and roasting processes

Selective leaching behavior of the spent NdFeB magnets was investigated to find out how controlled phase system through the roasting conditions gave an impact on the performance of the selective leaching. The pre-formed Nd2O3 by the selective oxidation made it possible to prevent the formation of NdFeO3 at high roasting temperature. This resulted in the ideal Nd2O3 and Fe2O3 phase system, which was obtained by roasting at 660 °C, suitable for the selective leaching of Nd. While the roasting at 600 °C was still not enough to get full oxidation, the roasting at 720 °C made the NdFeO3 formed. These characteristics with the roasting conditions affected leaching behavior. The NdFeB powder sample of 32 μm particle diameter, roasted at 600 °C showed the highest Nd leaching efficiency as well as the highest Fe leaching efficiency, which seemed to be ascribed to the existence of the metallic Fe. The poor leaching efficiency for the large powder size after roasting was ascribed to the poor diffusion characteristic of the H2SO4 solution. With the controlled phase system, the 100% leaching efficiency of Nd could be obtained by reducing the particle size to 16 μm. The formation of NdFeO3 as a co-product, which had resistance to the reaction with the leaching agent, could prevent the dissolution of Nd2O3 around the NdFeO3 layer. Thus, the 720 °C roasting condition showed the lowest leaching efficiency. The co-product Fe2O3 also showed good resistance to leaching so its leaching efficiency was just 5–6% after the leaching time of 3–4 h.

Achievement of Sub‐Diffractive Detection Depth in Absorption Spectroscopy Using Excitation from an Upconverting Particle

Conventionally, a collimated visible laser beam can only be focused to a transverse region volume with a waist of about 200 nm and an axial waist of about 1200 nm due to the wave nature of light. Several techniques have been used to bypass the diffraction limit, including a recently developed one using the emission from an optically trapped upconverting nanoparticle. This nanoparticle has a diameter smaller than 200 nm, such that it emits like a dipole into a 45° cone. Thus, not only is the emission coming from a particle smaller in size than the waist of the diffraction‐limited spot but also the cone is smaller than that of the volume of a very tightly focused beam. Here, the technique is developed even further where the emission coming from a specific region of the cone is selected by an optical fiber‐based pinhole in the detection path. Using this technique, a confocal depth of about 200 nm is achieved as the overlap between the emission cone and the detection volume. This would correspond to a volume of about 250 attoliters for a 1.5 μm diameter particle which can be reduced to 40 attoliters by using a 500 nm diameter particle.

Investigation of an indigenous chalcopyrite ore leaching in ammonia solution: characterization, leaching and kinetics

ABSTRACT Chalcopyrite ore is one of the most abundant and pertinent oxidized copper minerals. In this research, the dissolution kinetics of chalcopyrite in an ammonia solution was examined. During leaching, the influences of leachant concentration, temperature, and particle diameter on the extent of copper ore dissolution were investigated. However, it was affirmed that the dissolution efficiency of chalcopyrite ore increased with decreasing particle fraction and increasing reaction temperature and ammonia concentration. About 68.6% copper ore dissolution was achieved with 2.0 mol/L NH3, 75 ºC reaction temperature, and 45 μm particle diameter within 120 minutes. The dissolution reaction mechanism was found to be described by diffusion-control with a calculated activation energy of 32.26 kJ/mol. In the XRD spectra of the residual product obtained at established conditions, CuFeS2 peaks were absent, indicating the leachability of the sample. Hence, the leach residue could serve as an important by-product for some local industries.

Association between sea-land breeze and particulate matter in five coastal urban locations in India

Particulate matter less than 2.5 μm particle diameter (PM2.5) is the most significant environmental issue globally. PM2.5 is an integral component of air quality monitoring and management, human health, weather, climate, and epidemiological research. In this work, we investigate the seasonal variation in PM2.5 mass concentrations and the association between the sea-land breeze system and particulate matter in five coastal urban locations in India (Kolkata, Visakhapatnam, Chennai, Thiruvananthapuram, and Mumbai). The relative occurrence of high PM2.5 mass concentrations was the greatest during the winter season (December through February) while the relative occurrence of low PM2.5 mass concentrations was the greatest during the monsoon season (June through September). Amongst locations, Kolkata experiences the highest PM2.5 loading in winter while Thiruvananthapuram experiences the lowest PM2.5 loading in monsoon. Indo-Gangetic Plain (IGP) outflow onto the Bay of Bengal significantly impacts locations along the eastern coast of India with reduced impact from north (Kolkata) to south (Chennai). The sea-breeze component analysis revealed daily cycles of the sea-land breeze with varying magnitudes of the breeze between the different seasons. Overall, we found a negative association between the sea-land breeze magnitude and PM2.5 mass concentrations, implying that the weakened sea-land breeze may deteriorate air quality in coastal locations due to poor ventilation. The vertical profiles of aerosol extinction showed elevated aerosol layers within 1 km from the surface in almost all locations. The decreasing trend in the land-sea temperature contrast in coastal locations is expected to deteriorate air quality in coastal locations in the warming future. Nevertheless, critical analyses using ground-based remote sensing techniques are required for a better understanding the impact of sea-land breeze dynamics on air quality in coastal locations.

Development of a Microfluidic Device for Blood Cells Extraction in Liquid Biopsy

This project aims to produce a microfluidic device capable of separating 6 μm and 20 μm diameters particles by inertial sorting. This Lab-on-Chip (LoC) was designed with a trapezoidal cross-section for better fluid control and effective particle manipulation at the microscopic level, as demonstrated by COMSOL simulations. The device was manufactured on a substrate of Polymethyl Methacrylate (PMMA) by femtosecond laser technology and then assembled using an innovative geometry-preserving Isopropyl alcohol-based procedure. The LoC was test with spherical plastic microparticles of two diameters (6 μm and 20 μm) suspended in distilled water. The separation efficiencies were (98.2 ± 1.6) % for 20 μm diameter particles and (70.0 ± 1.8) % for 6 μm diameter particles in good agreement with the simulation results. Finally, after a microfluidic channels’ acetone vapors treatment, the device demonstrated a good ability to separate biological particles (Red Blood Cells) at different concentrations (20%, 30%, 40%, 50%) in a PBS buffer.

Oxidation of fine aluminum particles: thermally induced transformations in particle shells and kinetics of oxide nucleation.

This paper investigates the process of oxidation of fine aluminum powder, consisting of spherical Al particles of 'metal core/oxide shell' type, when heated in air at temperatures below 550 °C. The highly dispersed aluminum powder 'Alex' used in this work (particle size: 0.05-1.5 μm and number average particle diameter (DN): 0.11 μm) was produced by electric explosion of a thin Al wire in argon with subsequent passivation in an oxygen-containing atmosphere. For the first time, the influence of the particle size on the oxidation process has been identified. During the reaction, individual γ-Al2O3 oxide nuclei grow at the surface of Al particles with diameters less than 300 nm without laterally overlapping to form a protective passivating layer, as typically occurs during the oxidation of micron-sized particles or bulk metal. The localization of γ-Al2O3 nuclei is determined by the regions where peeling of the primary amorphous oxide film from the surface of the metal core of an Al particle occurs due to the thermal decomposition of aluminum hydroxides (T ≈ 350 °C) present within the particle shells. A significant increase in the contributions of the following factors leads to a high oxidation rate: the diffusion within the disordered structure of a particle core and the surface diffusion of cations (Ea = 80.6 ± 5.3 kJ mol-1, 400-450 °C), the surface and grain boundary diffusion of oxygen during the growth of γ-Al2O3 crystallites (Ea = 108.3 ± 11.2 kJ mol-1, 470-500 °C) and the surface and grain boundary transport of anions through an amorphous and underlying nanocrystalline oxide layer with a constant thickness (Ea = 205.1 ± 8.6 kJ mol-1, 520-550 °C). The results obtained make it possible to expand the theoretical understanding of the manifestations of the size effect in solid-phase reactions and take into account its influence in practice.

Towards optical MAS magnetic resonance using optical traps

Higher magic angle spinning (MAS) frequencies than currently available are desirable to improve spectral resolution in NMR and EPR systems. While conventional strategies employ pneumatic spinning limited by fluid dynamics, this paper demonstrates the development of an optical spinning technique in which vacuum quality dictates the maximum achievable spinning frequency. Using optical traps, we levitated a range of micron-sized samples. Under vacuum we achieved optical rotation of a single ∼10 μm diameter particle of vaterite at several mbar up to hundreds of Hz and of 20 μm diameter SiO2 particles at ≤10−2 mbar at several kHz. At ambient conditions, we optically levitated γ-irradiated alanine particles of 20–50 μm diameter. Additionally, using a single chip EPR detector operating at 11 GHz, we measured the EPR spectrum for a 30 μm γ-irradiated alanine particle in contact with the chip surface (i.e., without optical levitation) in a single scan lasting 92 s. These observations suggest that a γ-irradiated alanine particle having a diameter in the order of 30 μm is a promising candidate for our aim of demonstrating the first magnetic resonance experiment on optically levitated samples. Furthermore, we discuss strategies, limitations, and the potential of implementing MAS with optical traps for NMR and EPR.

Intra-event evolution of elemental and ionic concentrations in wet deposition in an urban environment

Abstract. A measurement campaign was conducted in the Paris region, focusing on the evolution of chemical composition of wet deposition during rainfall events from sequential sampling. A total of eight rain events were documented and characterized by varying meteorological conditions, atmospheric dynamics, and aerosol particle concentrations representative of urban conditions and influenced by long-range mineral dust transport. The intra-event evolution of the chemical composition of wet deposition revealed the predominant role of meteorological parameters and local sources in the observed mass concentration variability. From selected case studies, the washout ratios (WRs) and scavenging coefficients were quantified by conducting simultaneous measurements of aerosol particle composition and wet deposition. The results highlighted a variability of the WR and scavenging coefficients depending on the rainfall rate and on the chemical species. Scavenging coefficients estimated from WR ranged from 5.4×10-8 to 1.1×10-5 s−1 for chemical elements, and they are within the range of values reported in the literature for 0.2–2 µm particle diameters. Our results pointed out that the scavenging coefficient increases with rainfall rate according to a power law, as previously shown in the literature, indicating a stronger removal of particles from the atmosphere with greater precipitation intensity. Quantitative analysis of the data allowed us to estimate the relative contributions of in-cloud scavenging (ICS) for selected rain events. The ICS relative contributions ranged on average from 23 % to 62 % depending on the rain events, and they varied according to the chemical species within the same rain event. This highlights the variability and complexity of the wet deposition process and the influence of specific factors on the contribution of ICS, such as aerosol particle size and hygroscopicity. Overall, this study highlights the variability of wet deposition and its chemical composition and the need to consider the specificities of each event to fully understand the underlying mechanisms.

Diathermy and bone sawing are high aerosol yield procedures.

Orthopaedic surgery uses many varied instruments with high-speed, high-impact, thermal energy and sometimes heavy instruments, all of which potentially result in aerosolization of contaminated blood, tissue, and bone, raising concerns for clinicians' health. This study quantifies the aerosol exposure by measuring the number and size distribution of the particles reaching the lead surgeon during key orthopaedic operations. The aerosol yield from 17 orthopaedic open surgeries (on the knee, hip, and shoulder) was recorded at the position of the lead surgeon using an Aerodynamic Particle Sizer (APS; 0.5 to 20 μm diameter particles) sampling at 1 s time resolution. Through timestamping, detected aerosol was attributed to specific procedures. Diathermy (electrocautery) and oscillating bone saw use had a high aerosol yield (> 100 particles detected per s) consistent with high exposure to aerosol in the respirable range (< 5 µm) for the lead surgeon. Pulsed lavage, reaming, osteotome use, and jig application/removal were medium aerosol yield (10 to 100 particles s-1). However, pulsed lavage aerosol was largely attributed to the saline jet, osteotome use was always brief, and jig application/removal had a large variability in the associated aerosol yield. Suctioning (with/without saline irrigation) had a low aerosol yield (< 10 particles s-1). Most surprisingly, other high-speed procedures, such as drilling and screwing, had low aerosol yields. This work suggests that additional precautions should be recommended for diathermy and bone sawing, such as enhanced personal protective equipment or the use of suction devices to reduce exposure.

Polymer-insertion Effect on Urea Conversion Kinetics via Enzymes Immobilized on Magnetic Microparticles

Urease was covalently immobilized on the magnetic particles without and with polymer between the urease and the particle. The polymer insertion enhanced the conversion from urea to bicarbonate. The ureases were immobilized on the magnetic microparticles through covalent bonds. 150 μL of stock solution of 3 μm diameter particles was washed three times with 20 mM MES rubbing solution at pH 6.0. The results of this study seem to be useful in designing a reactor for recycling wastewater generated in the semiconductor process.

Development and Comparative Evaluation of Two Different Label-Free and Sensitive Fluorescence Platforms for Analysis of Olaparib: A Recently FDA-Approved Drug for the Treatment of Ovarian and Breast Cancer.

Olaparib (OLA) is a PARP inhibitor drug which has been recently approved by the Food and Drug Administration (FDA) for the treatment of ovarian and breast cancer. A convenient analytical tool for the quantitation of OLA in its dosage form and plasma samples was urgently needed. This study describes, for the first time, the development of two different label-free and sensitive fluorescence-based platforms for the pharmaceutical and bioanalysis of OLA. These platforms were microwell-assisted with a fluorescence microplate reader (MW-FLR) and high-performance liquid chromatography with fluorescence detection (HPLC-FD). Both MW-FLR and HPLC-FD employed the native fluorescence of OLA as an analytical signal. The MW-FLR involved measuring the fluorescence signals in 96-well white-opaque plates. The HPLC-FD involved chromatographic separation of OLA and duvelisib (DUV), as an internal standard on a Nucleosil-CN HPLC column (250 mm length × 4.6 mm i.d., 5 µm particle diameter) with a mobile phase composed of acetonitrile: water (25:75, v/v) pumped at a flow rate of 1.7 mL/min. Elution of OLA and DUV was detected using a fluorescence detector. The optimal conditions of both MW-FLR and HPLC-FD were established, and they were validated according to the guidelines of the International Council for Harmonization for the validation of analytical procedures. The linear ranges of MW-FLR and HPLC-FD were 25-1000 and 5-200 ng/mL, respectively, with limits of detection of 15 and 1.7 ng/mL, respectively. The accuracy and precision of both platforms were confirmed as the recovery values were ≥98.2% and the relative standard deviations (RSD) were ≤2.89%. Both methodologies were satisfactorily applied to the quantitation of OLA in its commercial dosage form (Lynparza® tablets) and plasma samples with high accuracy and precision. The greenness of both MW-FLR and HPLC-FD was assessed using two different multiple parameter-based metric tools, and the results proved their greenness and adherence to the requirements of green analytical approaches. Both platforms have simple procedures and acceptable levels of analytical throughput. In conclusion, the proposed MW-FLR and HPLC-FD are valuable tools for routine use in quality control and clinical laboratories for the quantitation of OLA for the purposes of pharmaceutical quality control, pharmacokinetic studies, and bioequivalence testing.

Understanding the Transition from High-Selective to High-Efficient Chiral Separations by Changing the Organic Modifier with Zwitterionic-Teicoplanin Chiral Stationary Phase.

The retention behavior of small molecules and N-protected amino acids on a zwitterionic teicoplanin chiral stationary phase (CSP), prepared on superficially porous particles (SPPs) of 2.0 μm particle diameter, has shown that efficiency and enantioselectivity, and so enantioresolution, dramatically change depending on the employed organic modifier. In particular, it was found that while methanol permits the boost of enantioselectivity and resolution of the amino acids, at the cost of efficiency, acetonitrile allows for the ability to reach extraordinary efficiency even at high flow rates (with reduced plate height <2 and up to 300,000 plates/m at the optimum flow rate). To understand these features, an approach based on the investigation of mass transfer through the CSP, the estimation of the binding constants of amino acids on the CSP, and the assessment of compositional properties of the interfacial region between bulk mobile phase and solid surface has been adopted.

Evaluation of structural parameters to predict particle filtration and air permeability performance of woven textiles

The COVID-19 pandemic has highlighted environmental and supply issues related to single-use protective masks for both the general public and some healthcare workers. Reusable fabrics are an interesting alternative to disposable nonwovens and offer a prospect of protection in other fields such as against fine particles in urban areas. In this paper, the behavior of 22 woven fabrics regarding air permeability, simulating breathability through the material, and filtration against 3 µm diameter particles is investigated. First, basic laws are verified between the performance of a single layer of fabrics and that of a stack. A relationship is established between air permeability and filtration efficiency, allowing one to be calculated when the other is known. Second, the influence of parameters defined at various scales of the structure (fibers, yarns and fabrics) is analyzed. The most sensitive structural parameters that can be considered as predictors are then identified and used in a model allowing the calculation of air permeability. In this model two levels of porosity are taken into account: a macroscopic porosity at the scale of the woven structure and a microscopic porosity at the scale of the thread. The model proposed in this study offers a convenient method to design an effective filter from data easily measurable during manufacturing.

Modeling a pesticide remediation strategy for preparative liquid chromatography using high-performance liquid chromatography

BackgroundCannabis sativa L. also known as industrial hemp, is primarily cultivated as source material for cannabinoids cannabidiol (CBD) and ∆9-tetrahydrocannabinol (∆9-THC). Pesticide contamination during plant growth is a common issue in the cannabis industry which can render plant biomass and products made from contaminated material unusable. Remediation strategies to ensure safety compliance are vital to the industry, and special consideration should be given to methods that are non-destructive to concomitant cannabinoids. Preparative liquid chromatography (PLC) is an attractive strategy for remediating pesticide contaminants while also facilitating targeted isolation cannabinoids in cannabis biomass.MethodsThe present study evaluated the benchtop-scale suitability of pesticide remediation by liquid chromatographic eluent fractionation, by comparing retention times of 11 pesticides relative to 26 cannabinoids. The ten pesticides evaluated for retention times are clothianidin, imidacloprid, piperonyl butoxide, pyrethrins (I/II mixture), diuron, permethrin, boscalid, carbaryl, spinosyn A, and myclobutanil. Analytes were separated prior to quantification on an Agilent Infinity II 1260 high performance liquid chromatography with diode array detection (HPLC-DAD). The detection wavelengths used were 208, 220, 230, and 240 nm. Primary studies were performed using an Agilent InfinityLab Poroshell 120 EC-C18 3.0 × 50 mm column with 2.7 μm particle diameter, using a binary gradient. Preliminary studies on Phenomenex Luna 10 μm C18 PREP stationary phase were performed using a 150 × 4.6 mm column.ResultsThe retention times of standards and cannabis matrices were evaluated. The matrices used were raw cannabis flower, ethanol crude extract, CO2 crude extract, distillate, distillation mother liquors, and distillation bottoms. The pesticides clothianidin, imidacloprid, carbaryl, diuron, spinosyn A, and myclobutanil eluted in the first 3.6 min, and all cannabinoids (except for 7-OH-CBD) eluted in the final 12.6 min of the 19-minute gradient for all matrices evaluated. The elution times of 7-OH-CBD and boscalid were 3.44 and 3.55 min, respectively.Discussion7-OH-CBD is a metabolite of CBD and was not observed in the cannabis matrices evaluated. Thus, the present method is suitable for separating 7/11 pesticides and 25/26 cannabinoids tested in the six cannabis matrices tested. 7-OH-CBD, pyrethrins I and II (RTA: 6.8 min, RTB: 10.5 min), permethrin (RTA: 11.9 min, RTB: 12.2 min), and piperonyl butoxide (RTA: 8.3 min, RTB: 11.7 min), will require additional fractionation or purification steps.ConclusionsThe benchtop method was demonstrated have congruent elution profiles using preparative-scale stationary phase. The resolution of pesticides from cannabinoids in this method indicates that eluent fractionation is a highly attractive industrial solution for pesticide remediation of contaminated cannabis materials and targeted isolation of cannabinoids.

Characterisation of hydrodynamic trapping in microfluidic cross-slot devices for high strain rate applications.

Hydrodynamic trapping of a particle or cluster of particles based on contact and non-contact approaches has brought prominent insights to micro-nano scale applications. Of the non-contact methods, image-based real-time control in cross-slot microfluidic devices is one of the most promising potential platform for single cellular assays. Here, we report results from experiments conducted in two cross-slot microfluidic channels of different widths, with varying real-time delay of the control algorithm and different magnification. Sustained trapping of 5 μm diameter particles was achieved with high strain rates, of order 102 s-1, higher than in any previous studies. Our experiments show that the maximum attainable strain rate is a function of the real-time delay of the control algorithm and the particle resolution (pixel/μm). Therefore, we anticipate that with further reduced time delays and enhanced particle resolution, considerably higher strain rates can be attained, opening the platform to single cellular assay studies where very high strain rates are required.

Unpacking Intermineral Synergies and Reactions During Dust Deposition in an Impingement Coolant Jet

Abstract This paper seeks to unpack synergies that exist between minerals during deposition of the heterogeneous AFRL02 mixture in gas turbine engines and demonstrate that the contributions of each mineral cannot be considered independently. In each experiment, one gram of mineral dust (0–10 µm particle diameter distribution) was injected into an 894 K, 57 m/s coolant flow impinging normally on a Hastelloy X plate with a surface temperature of 1033 K, 1144 K, or 1255 K. Capture efficiency measurements, deposit morphology analyses, and X-ray diffraction results are reported. Besides AFRL02, single mineral dusts, dual mineral dusts, and AFRL02-like dust blends lacking in one mineral were tested. The results of the experiments elucidate that the deposition behavior of single minerals indeed cannot explain the composite deposition of heterogeneous mixtures. For example, gypsum had the highest capture efficiency of any single mineral in ARFL02, and yet removing gypsum from AFRL02 counterintuitively raised the capture efficiency of that blend when compared to AFRL02. Quartz was found to erode albite deposits but stick to and build upon dolomite and halite deposits, even though quartz did not deposit significantly as a single mineral. Quartz also chemically reacted with gypsum and dolomite to form wollastonite and diopside, respectively. Finally, we found that the capture efficiency of each blend increased with plate temperature, but not according to the same trend. Results are interpreted through the lens of CaO–MgO–Al2O3–SiO2 eutectic chemistry, but the chemical pathways by which these eutectics come into existence is found to be of equal importance.

Impact of particle diameter and thermal radiation on the explosion of dust layers

Numerical simulations were performed to study the impact of thermal radiation and particle diameter on layered coal-dust explosions. The geometrical setup considered the interaction of a primary explosion with a thin layer of coal dust inside of a closed channel. The simulations solved the compressible reacting Navier–Stokes equations coupled to an Eulerian granular multiphase model. Thermal radiation was included by solving the radiation transfer equation using the filtered spherical harmonics approximation. The results show that the impact of radiation on the dust explosion is situation specific. Radiation can promote, inhibit, or have little impact on the explosion depending on the particle diameter. Radiation has a slight inhibiting effect on dust layers comprised of 30 and 100 μm-diameter coal particles. Radiation quenched the explosion when particles were 5 μm in diameter. Radiation promoted stable burning for larger 150 μm-diameter coal particles, while simulations excluding radiation for 150 μm-diameter coal particles produced a failed explosion. The influence of particle diameter on the dispersibility characteristics of dust layers has a significant impact on the explosion. Small 5 μm-diameter coal particles are dispersed poorly by the leading shock and are too highly concentrated to burn. Large 150 μm-diameter particles disperse higher into the channel and show improved mixing, but have large thermal time scales that inhibit vigorous reaction. Cases with 30 and 100 μm-diameter particles show a good compromise between dispersibility, mixing, and thermal time scales which produce stable combustion with or without the inclusion of thermal radiation in the model.

Separation of nadolol racemates by high pH reversed-phase fixed-bed and simulated moving bed chromatography

The separation of nadolol racemates under high pH reversed-phase using both the fixed-bed (FB) and the simulated moving bed (SMB) preparative chromatographic techniques is reported after the previous published work [1] where the Waters XBridge C18 adsorbent and an ethanol:water:diethylamine solvent mixture were validated to allow the separation of the multicomponent feed mixture composed by four nadolol stereoisomers into two pure racemates (two pairs of enantiomers).In this work, the experimental preparative separations using one commercial fixed-bed preparative HPLC Azura system equipped with one sole column of preparative dimensions (30 mm ID × 250 mm L) and one lab-scale SMB apparatus (the FlexSMB-LSRE pilot unit) equipped with six semi-preparative columns (19 mm ID × 100 mm L) are presented. Both systems use the Waters XBridge C18 adsorbent of 10 μm particle diameter. The screening of the mobile phase composition elected the 30:70:0.1 (v/v/v) ethanol:water:diethylamine solvent mixture to perform both FB and SMB preparative operations.A large set of experimental, modelling and simulation results are presented, including pulses, measurement and modelling of the adsorption equilibrium isotherms, and its validation through breakthroughs measurements. The modelling and simulation steps allowed the prediction and the optimization of both the FB and SMB operating conditions.For FB, using a feed concentration of 9 g/L of an equimolar mixture of the two nadolol racemates, both were recovered almost pure (at least 99.9 %), with a global system productivity of 3.06 gfeed/(Lbed.hr) and a solvent consumption of 4.21 Lsolvent/gfeed. For SMB, the pilot unit’s pressure drops limits imposed a maximum internal flow-rate of only 5 mL/min and, for a nadolol feed concentration of 2 g/L, both racemates were recovered 100 % pure, with a system productivity of 0.13 gfeed/(Lbed.hr) and a solvent consumption of 6.19 Lsolvent/gfeed. Additional simulation results showed that a SMB preparative unit can perform the 9 g/L nadolol racemate separation with a system productivity of 3.61 gfeed/(Lbed.hr) and a solvent consumption of only 1.95 Lsolvent/gfeed using the same average internal flow-rate as in FB operation. Even better SMB productivities can still be obtained using the same feed or solvent flow-rates as in FB operation if the internal SMB flow-rates are allowed and not limited by the system pressure drop.The experimental results presented in this work validate the strategy of separating a four nadolol stereoisomers mixture into two pure nadolol racemates, each one composed by a pair of nadolol enantiomers, using an achiral C18 adsorbent through FB and SMB chromatographic techniques. Each nadolol racemate can later be purified into pure nadolol stereoisomers using standard binary chiral FB and SMB chromatography. In this way, this works introduces a real and experimental solution for the complete multicomponent preparative separation of the four nadolol stereoisomers.