Investigation of Absorption and Scattering Properties of Soot Aggregates of Different Fractal Dimension at 532 nm Using RDG and GMM

Radiative properties of numerically generated fractal soot aggregates of different fractal dimensions were studied using the numerically accurate generalized Mie-solution method (GMM) and the Rayleigh-Debye-Gans (RDG) approximate theory. Fractal aggregates of identical prefactor but different fractal dimensions, namely, 1.4, 1.78, and 2.1, were generated numerically using a tunable algorithm of cluster–cluster aggregation for aggregates containing up to 800 primary particles. Radiative properties of these aggregates were calculated at a wavelength of 532 nm assuming a soot refractive index of 1.6 + 0.6i. Four commonly used structure factors in the RDG approximation were used to investigate the effect of structure factor on the differential and total scattering cross-sections and the asymmetry factor. The differential and total scattering properties calculated using the RDG approximation become increasingly sensitive to the structure factor with increasing the fractal dimension. Primary particle interactions are the fundamental mechanism for the aggregate absorption enhancement for small aggregates and the shielding effect for larger aggregates. The extent of these two competing factors is dependent on the fractal dimension and aggregate size. RDG reasonably predicts the effect of fractal dimension on the scattering properties, but fails to account for the effect of aggregation or fractal morphology on the absorption property of fractal soot aggregates, though the error is in general less than 15%.

Copyright 2013 American Association for Aerosol Research     

Influence of OH− concentration on the illitization of kaolinite at high pressure

The products of hydrothermal reactions of kaolinite at 300 °C and 1000 bars were studied in KOH solutions covering an OH^? concentration, [OH^?], of 1 M to 3.5 M. XRD patterns indicated a notable influence of the [OH^?] on the reaction. At [OH] ≥ 3 M, the only stable phase was muscovite/illite. The content of muscovite/illite was calculated from the analysis of the diagnostic 060 reflections of kaolinite and muscovite/illite. The results showed a linear dependence of kaolinite and muscovite/illite contents with [OH^?]. ²⁷Al MAS NMR spectroscopy revealed the formation of small nuclei of K-F zeolite at high [OH^?]. Finally, modelling of the ²⁹Si MAS NMR spectra indicated that the Si/Al ratio of the muscovite/illite formed was very close to that of muscovite, at least in the mineral formed at low [OH^?]. In good agreement with the XRD data, the quantification of the reaction products by ²⁹Si MAS NMR indicated a linear decrease of the kaolinite content with increasing OH^? concentration.     

In-situ characterization of e-cigarette aerosols by 90°-light scattering of polarized light

The polarization ratio method is used for fast in-situ characterization of unimodal condensed aerosols of e-cigarettes. The method is based on 90°-light scattering of polarized 680 nm laser light by the droplet ensemble inside an optically defined measuring volume. Mass median droplet diameter (MMD) is derived from the ratio of scattered light from horizontally and vertically polarized incident light beams assuming a fixed value of the geometric standard deviation of the aerosol mass distribution. MMD is used to correct for the size dependence of the mass-based scattering signal of vertically polarized light to obtain the mass concentration if the sensor is calibrated once with an aerosol with a fixed MMD. The sensor uses commercially available aerosol photometers, and its application to e-cigarette aerosols was validated with an impactor for MMD and with a filter measurement for mass concentration. Good correlation (r² > 0.97) for both parameters was observed. Application ranges are mass concentration range 0.5–50 mg/L, MMD 0.2–1.2 µm, 100 ms time resolution, and 0.2–3 L/min flow rate. The usefulness of this simple sensor for e-cigarette aerosol characterization is demonstrated by developing a scaling law between MMD and operating parameters of an e-cigarette, i.e., puff flow rate and mass concentration.

Copyright © 2018 American Association for Aerosol Research     

Study of autocorrelation function of polymer and polymer–nanocomposite solutions using dynamic light scattering method

Dynamic light scattering (DLS) of polymer and polymer–nanocomposite solutions has been performed to examine the effect in the morphology of polymer solution in presence of nanoparticles analyzing their correlation functions. The size of the nanoparticle was determined using UV–Vis absorption spectroscopy measurements. Analysis of the correlation functions of polymer solution shows existence of two modes, namely, fast and slow modes, along with the distinct values in their corresponding amplitudes and relaxation times. Interestingly, the fast mode of the solution was found to smear out, enhancing the slow mode when we grow nanoparticles into the polymer solution. Apart from the above study, the temperature variation study of both the solutions show that above and below room temperature, the polymer solution becomes more heterogeneous compared to the solution when nanoparticles are grown into it.     

First measurements of the number size distribution of 1–2 nm aerosol particles released from manufacturing processes in a cleanroom environment

This study was conducted to observe a potential formation and/or release of aerosol particles related to manufacturing processes inside a cleanroom. We introduce a novel technique to monitor airborne sub 2 nm particles in the cleanroom and present results from a measurement campaign during which the total particle number concentration (>1 nm and >7 nm) and the size resolved concentration in the 1 to 2 nm size range were measured. Measurements were carried out in locations where atomic layer deposition (ALD), sputtering, and lithography processes were conducted, with a wide variety of starting materials. During our campaign in the clean room, we observed several time periods when the particle number concentration was 10⁵ cm^?3 in the sub 2 nm size range and 10⁴ cm^?3 in the size class larger than 7 nm in one of the sampling locations. The highest concentrations were related to the maintenance processes of the manufacturing machines, which were conducted regularly in that specific location. Our measurements show that around 500 cm^?3 sub 2 nm particles or clusters were in practice always present in this specific cleanroom, while the concentration of particles larger than 2 nm was less than 2 cm^?3. During active processes, the concentrations of sub 2 nm particles could rise to over 10⁵ cm^?3 due to an active new particle formation. The new particle formation was most likely induced by a combination of the supersaturated vapors, released from the machines, and the very low existing condensation sink, leading to pretty high formation rates J_{1.4 nm} = (9 ± 4) cm^?3 s^?1 and growth rates of particles (GR_{1.1–1.3 nm} = (6 ± 3) nm/h and GR_{1.3–1.8 nm} = (14 ± 3) nm/h).

Copyright © 2017 American Association for Aerosol Research     

Investigation of vehicle exhaust sub-23 nm particle emissions

A solid particle number limit was applied to the European legislation for diesel vehicles in 2011. Extension to gasoline direct injection vehicles raised concerns because many studies found particles below the lower size limit of the method (23 nm). Here we investigated experimentally the feasibility of lowering this size. A nano condensation nucleus counter system (nCNC) (d_50% = 1.3 nm) was used in parallel with condensation particle counters (CPCs) (d_50% = 3 nm, 10 nm and 23 nm) at various sampling systems based on ejector or rotating disk diluters and having thermal pre-treatment systems consisting of evaporation tubes or catalytic strippers. An engine exhaust particle sizer (EEPS) measured the particle size distributions. Depending on the losses and thermal pre-treatment of the sampling system, differences of up to 150% could be seen on the final detected particle concentrations when including the particles smaller than 23 nm in diameter. A volatile artefact as particles with diameters below 10 nm was at times observed during the cold start measurements of a 2-stroke moped. The diesel vehicles equipped with the Diesel Particulate Filter (DPF) had a low solid sub-23 nm particles fraction (<20%), the gasoline with direct injection vehicles had higher (35–50%), the gasoline vehicles with port fuel injection and the two mopeds (two and four-stroke) had the majority of particles below 23 nm. The size distributions peaked at 60–80 nm for the DPF equipped vehicles, at 40–90 nm for the gasoline vehicles with a separate nucleation mode peak at approximately 10 nm sometimes. Mopeds peaked at sizes below 50 nm when their aerosol was thermally pre-treated.

© 2017 American Association for Aerosol Research     

Mobility Analysis of 2 nm to 11 nm Aerosol Particles with an Aspirating Drift Tube Ion Mobility Spectrometer

We describe the performance of a drift tube-ion mobility spectrometry (DT-IMS) instrument for the measurement of aerosol particles. In DT-IMS, the electrical mobility of a measured particle is inferred directly from the time required for the particle to traverse a drift region, with motion driven by an electrostatic field. Electrical mobility distributions are hence linked to arrival time distributions (ATDs) for particles reaching a detector downstream of the drift region. The developed instrument addresses two obstacles that have limited DT-IMS use for aerosol measurement previously: (1) conventional drift tubes cannot efficiently sample charged particles at ground potential and (2) the sensitivities of commonly used Faraday plate detectors are too low for most aerosols. Obstacle (1) is circumvented by creating a “sample volume” of aerosol for measurement, defined by the streamlines of fluid flow. Obstacle (2) is bypassed by interfacing the end of the drift region with a condensation particle counter. The DT-IMS prototype shows high linearity for arrival time versus inverse electrical mobility (R ² > 0.99) over the size range tested (2.2–11.1 nm), and measurements compare well with both analytical and numerical models of device performance. A dimensionless calibration curve linking drift time to inverse electrical mobility is developed. In less than 5 s, it is possible to measure 11.1 nm particles, while 2.2 nm particles are analyzable on a subsecond scale. The transmission efficiency is found to be dependent upon electrostatic deposition for short drift times and upon advective losses for long drift times.

Copyright 2014 American Association for Aerosol Research     

Comparison of heat- and pressure-induced gelation of β-lactoglobulin aqueous solutions studied by small-angle neutron and dynamic light scattering

The gelation mechanism of β-lactoglobulin (bLG) aqueous solutions was investigated by dynamic light scattering (DLS) and small-angle neutron scattering (SANS). Temperature- and pressure-jump experiments, respectively, abbreviated as T-jump (from 20 to 75 °C; T-jump) and P-jump (from 0.1 to 315 MPa) were carried out and the time evolution of gel structure was monitored by DLS and SANS as a function of time. The gelation threshold was determined by DLS as the point when nonergodicity appeared. In the case of T-jump, a rapid increase of the time-average scattered intensity, 〈I〉_T, and a steep decrease of the initial amplitude of the intensity-intensity time correlation function, , were observed at the gelation threshold. On the other hand, P-jump showed a gradual increase of the 〈I〉_T and a continuous decrease of the . It was revealed by SANS that bLG underwent thermal denaturation, resulting in a formation of gels consisting of densely aggregated unfolded bLG oligomers. On the other hand, the pressure-induced gels were found to be a fractal aggregates consisting of primary particles of bLG monomers. The difference in the gel structure as well as gelation mechanism between bLGs treated by T-jump and P-jump is discussed in comparison with T-induced and P-induced microphase separation of amphiphilic block copolymers in water [Osaka N, Shibayama M. Phys Rev Lett 2006;96:048303].     

Small Molecule Crystallography in the Laboratory of Organic Chemistry at ETH Zürich

The development of small-molecule crystallography in the Laboratory of Organic Chemistry (LOC) at ETH since its foundation by Jack Dunitz in 1957 is reported. We briefly review the scientific path of Dunitz before coming to ETH and subsequently illustrate research highlights until his retirement in 1990. Together with his doctoral students and postdoctoral fellows, Dunitz developed X-ray crystallography as a tool for studying chemical reactivity and reaction mechanisms, stereochemical, and in particular, conformational analysis, and supramolecular interactions. He hosted numerous leaders in the field in Zurich. After retirement, Dunitz remained highly research-active. The crystallography facilities were run in 1991–2013 by his former coworkers Bernd Schweizer and Paul Seiler. In 2013, the Small Molecule Crystallography Center (SMoCC) was founded by merging the X-ray facilities in inorganic and organic chemistry and its research-driven service is illustrated.     

Characterization and properties of iron-incorporated gismondine prepared at 80°C

Iron-incorporated zeolites were successfully synthesized at a low temperature such as 80°C by choosing appropriate starting materials and characterized by inductively coupled plasma atomic emission spectrometry (ICP-AES), wide-angle X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and magnetic susceptibility. ICP-AES showed␣that Fe component can be readily incorporated␣up to a maximum extent of Fe substitution, Fe/(Fe + Al) × 100 = 22.7%. XRD measurements suggested that the zeolites obtained have a crystal structure of gismondine type. The characterizations identified that the Fe component present in the products is all incorporated into the zeolite framework. The ammonia and water desorption profiles were compared for Fe-free and 22.7% Fe-zeolites ion-exchanged for NH₄⁺ by means of TG-MS and DSC. The ammonia desorption peak temperatures considerably shifted toward lower temperatures by the introduction of Fe, suggesting decreased solid acidity. DSC thermograms of the as-synthesized gismondines revealed that they do not contain free water (i.e., water not coordinated to cations) in the pores irrespective of the Fe content. The enhanced catalytic reactivity of the Fe-incorporated gismondines was also confirmed from the decomposition of hydrogen peroxide. An apparent activation energy of 43 kJ mol⁻¹ was obtained independent of the Fe contents in zeolites. This value was much lower than 70 kJ mol⁻¹ for the same reaction in the homogeneous solution containing iron alum as a reference sample.     

532 nm laser damage and nonlinear absorption of Cr2O72− doped KDP crystals

Potassium dihydrogen phosphate (KDP) single crystals doped with a series of trace dichromate (Cr₂O₇^2?) were prepared using “point seed” technique. The IR spectra suggest that the KDP crystal network becomes compact with trace of Cr₂O₇^2? while the lattice of crystal also can be destroyed by excessive doping. The UV–Vis spectra show that the transmittance percentage is descended of the doped KDP crystals. Z-scan analysis demonstrates that with increasing of Cr₂O₇^2? concentration, a gradual raise has been observed for the nonlinear absorption coefficient (β). The laser-induced damage threshold (LIDT) at 532 nm of the KDP crystal doped with 3000 ppm Cr₂O₇^2? is found to be 28.29 J/cm² which is higher than that of pure one under the R-on-1 model. However, as the doping concentration continues to increase, the LIDT decreases significantly. The variation of photoluminescence (PL) results is also consisted with the trend of LIDT for the doped samples. The LIDT of pyramidal sample is higher than that of prismatic one with the same doping concentration. The results suggest that the laser damage of doped crystal may be due to a synergistic effect of the concentration of micro defects and nonlinear absorption.     

Universal character of relaxation of the intensity of light scattering by boron oxide melt in the temperature range 300–340°C

It has been established that the process of stabilization of the boron oxide melt in the temperature range 300–340°С is accompanied by universal changes in the intensity of the polarized V _v component of light scattering characterized with the formation of a minimum. It has been demonstrated that the above feature does not depend on the direction of the intensity approaching to the stationary state for the selected temperature; i.e., it is observed in the process of intensity relaxation from both high and low temperatures. Upon attainment of the minimal values, the increase of the V _v intensity with the stabilization time was found to be satisfactorily described by the empirical dependence of the exponential type. The characteristic times of intensity changes calculated in accordance with the respective equation significantly exceed the times of structural relaxation and increase along with the temperature decrease in accordance with the exponential dependence. It has been established that the characteristic times of intensity changes as its values approach the stationary one from a higher temperature are larger than when approaching from a lower temperature. It has been shown that under these conditions, changes in the intensity of the depolarized H _v component are characterized with the formation of a maximum registered for both modes (sample cooling and heating). It has been revealed that the increase of the H _v intensity in the maximum does not exceed 10% of its regular value, which allows relating the formation of a minimum of the V _v component to the decrease of the isotropic light scattering intensity.     

Photodegradation of Natural Organic Matter in Water with UV Irradiation at 185 and 254 nm: Importance of Hydrodynamic Conditions on the Decomposition Rate

Abstract

The kinetic investigation of photodegradation of the natural organic matter (NOM) in natural lake water was conducted using two low‐pressure mercury lamps of the same nominal power: a) with suprasil quartz envelope emitting at both wavelengths ?254 nm and 185 nm (hereafter VUV); b) with standard quartz envelope emitting only at 254 nm (hereafter UV). In comparison to the UV process, the addition of 185 nm irradiation (VUV process) increased the degradation rate ten‐fold overall at lower and seventeen‐fold at higher Reynolds numbers, respectively. The hydrodynamic characteristics of the photoreactor are of crucial importance for total energy efficiency for VUV processes.     

Modeling light scattering by spherical pores for calculating the transmittance of transparent ceramics – All you need to know

In this paper transmittance predictions based on residual pore scattering in transparent ceramics with cubic crystallites via Mie theory and its approximations (Rayleigh, Fraunhofer, van de Hulst and Rayleigh-Gans, including the small- and large-size limits) are recalled and systematically compared. Due to the high phase contrast, the difference between different types of ceramics is of secondary importance, so that the essential conclusions are of general validity for all types of transparent ceramics. It is shown that the Rayleigh-Gans approximation and its large-size limit provide surprisingly good transmittance predictions, although it has not often been used in the ceramic literature. The main conclusion of this paper is that, of all the approximations presented here and used in ceramic science so far, the van de Hulst approximation is the one that most closely approaches the exact Mie results, although it has been largely ignored in the literature on transparent ceramics so far.     

Penetration of Sub-50 nm Nanoparticles Through Electret HVAC Filters Used in Residence

Pleated electret HVAC filters are often used in residence to mitigate the particles that originate both indoors and outdoors. These filters are usually tested with particles larger than 300 nm. However, residential particles can contain a significant amount of nanoparticles with size below 50 nm due to cooking, smoking, cleaning, wood burning, and outdoor infiltration. In order to characterize the nanoparticle removal by electret HVAC filters, penetrations of 3–50 nm silver nanoparticles through five different flat sheet electret media used in commercial residential HVAC filters were tested with face velocities of 0.05, 0.5, and 1.0 m s^–1. Experimental results showed that all media had significantly high penetrations with 0.35–0.8 at the most penetrating particle sizes (MPPSs) for all three velocities, which were in the sizes of 10–30 nm. A model based on single fiber theory for particle penetration predictions was used and compared with the experimental data. Results showed that the model predicted the nanoparticle penetrations very well for all media and all face velocities tested. According to the model, for enhancing the nanoparticle efficiency of the current commercial HVAC filters, the fiber diameter should be reduced or the number of pleats should be increased. However, by doing these, pressure drop and cost may be largely increased. On the other hand, this study found the existing commercial mechanical HVAC filters were much capable for sub–50 nm nanoparticle removal when their minimum efficiency reporting values (MERVs) were larger than 13 and it is concluded mechanical HVAC filters can do a better job than electret ones. However, the quality factor analysis showed electret filters could be regarded as the best filter media for removing particles smaller than 300 nm.

Copyright 2015 American Association for Aerosol Research     

Elastic properties and damping behavior of alumina–zirconia composites at room temperature

Alumina–zirconia composite ceramics (AZ composites) have been prepared in the whole range of compositions from pure alumina to zirconia (in steps of 10 vol.%) by slip casting, followed by sintering at 1350 °C and microstructural characterization via the Archimedes method (relative densities 0.93–0.99). Young's modulus has been measured at room temperature via the impulse excitation technique (IET) and, after appropriate porosity correction (linear, power-law, exponential), found to be in good agreement with the Hashin–Shtrikman bounds. The damping factor (internal friction), which has been measured for dense AZ composites (also via IET at room temperature), is found to increase with increasing zirconia content. Damping factors measured for porous AZ composites with porosities 25–71%, prepared with corn starch as a pore former, have been found to depend only slightly on porosity, unless the porosities are extremely high (>70%). At these porosities, however, where the Young's moduli approach zero, the damping factors exhibit a steep increase.     

Cohesive properties of refractory castable at 600 °C: Effect of sintering and testing temperature

This paper aims to evaluate cohesive properties for an alumina refractory with mullite-zirconia aggregates from wedge splitting tests (WST), and to assess their sensitivity to sintering and testing temperature. Five experiments were analyzed of which four were performed at 600^°C. The sought parameters were determined via weighted finite element model updating. The cohesive strength and the fracture energy were successfully calibrated and resulted in simulated data close to their experimental counterparts (i.e., between 4 and 11 times the measurement uncertainty). Increasing the sintering temperature from 1400^°C to 1450^°C enhanced the cohesion between the mullite-zirconia aggregates and the alumina matrix (20 % increase of the fracture energy and of the fracture process zone length). When the WSTs were performed at 600^°C, the cohesive strength was 10 % smaller while the fracture energy was 70 % higher than that at room temperature.     

Structural and physical properties of antibacterial Ag-doped nano-hydroxyapatite synthesized at 100°C

ABSTRACT: Synthesis of nanosized particle of Ag-doped hydroxyapatite with antibacterial properties is in the great interest in the development of new biomedical applications. In this article, we propose a method for synthesized the Ag-doped nanocrystalline hydroxyapatite. A silver-doped nanocrystalline hydroxyapatite was synthesized at 100°C in deionized water. Other phase or impurities were not observed. Silver-doped hydroxyapatite nanoparticles (Ag:HAp) were performed by setting the atomic ratio of Ag/[Ag + Ca] at 20% and [Ca + Ag]/P as 1.67. The X-ray diffraction studies demonstrate that powders made by co-precipitation at 100°C exhibit the apatite characteristics with good crystal structure and no new phase or impurity is found. The scanning electron microscopy (SEM) observations suggest that these materials present a little different morphology, which reveals a homogeneous aspect of the synthesized particles for all samples. The presence of calcium (Ca), phosphor (P), oxygen (O), and silver (Ag) in the Ag:HAp is confirmed by energy dispersive X-ray (EDAX) analysis. FT-IR and FT-Raman spectroscopies revealed that the presence of the various vibrational modes corresponds to phosphates and hydroxyl groups. The strain of Staphylococcus aureus was used to evaluate the antibacterial activity of the Ca10-xAgx(PO4)6(OH)2 (x = 0 and 0.2). In vitro bacterial adhesion study indicated a significant difference between HAp (x = 0) and Ag:HAp (x = 0.2). The Ag:Hap nanopowder showed higher inhibition.