81 research outputs found

    Neutron scattering study of magnetic ordering and excitations in the ternary rare-earth diborocarbide Ce^{11}B_2C_2

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    Neutron scattering experiments have been performed on the ternary rare-earth diborocarbide Ce11^{11}B2_2C2_2. The powder diffraction experiment confirms formation of a long-range magnetic order at TN=7.3T_{\rm N} = 7.3 K, where a sinusoidally modulated structure is realized with the modulation vector q=[0.167(3),0.167(3),0.114(3)]{\bm q} = [0.167(3), 0.167(3), 0.114(3)]. Inelastic excitation spectra in the paramagnetic phase comprise significantly broad quasielastic and inelastic peaks centered at ω0,8\hbar \omega \approx 0, 8 and 65 meV. Crystalline-electric-field (CEF) analysis satisfactorily reproduces the observed spectra, confirming their CEF origin. The broadness of the quasielastic peak indicates strong spin fluctuations due to coupling between localized 4f4f spins and conduction electrons in the paramagnetic phase. A prominent feature is suppression of the quasielastic fluctuations, and concomitant growth of a sharp inelastic peak in a low energy region below TNT_{\rm N}. This suggests dissociation of the conduction and localized 4f4f electrons on ordering, and contrasts the presently observed incommensurate phase with spin-density-wave order frequently seen in heavy fermion compounds, such as Ce(Ru1x_{1-x}Lax_x)2_2Si2_2.Comment: accepted for publication in Phys. Rev.

    Kaolinite particles as ice nuclei: learning from the use of different kaolinite samples and different coatings

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    Kaolinite particles from two different sources (Fluka and Clay Minerals Society (CMS)) were examined with respect to their ability to act as ice nuclei (IN). This was done in the water-subsaturated regime where often deposition ice nucleation is assumed to occur, and for water-supersaturated conditions, i.e., in the immersion freezing mode. Measurements were done using a flow tube (the Leipzig Aerosol Cloud Interaction Simulator, LACIS) and a continuous-flow diffusion chamber (CFDC). Pure and coated particles were used, with coating thicknesses of a few nanometers or less, where the coating consisted of levoglucosan, succinic acid or sulfuric acid. In general, it was found that the coatings strongly reduced deposition ice nucleation. Remaining ice formation in the water-subsaturated regime could be attributed to immersion freezing, with particles immersed in concentrated solutions formed by the coatings. In the immersion freezing mode, ice nucleation rate coefficients jhet from both instruments agreed well with each other, particularly when the residence times in the instruments were accounted for. Fluka kaolinite particles coated with either levoglucosan or succinic acid showed the same IN activity as pure Fluka kaolinite particles; i.e., it can be assumed that these two types of coating did not alter the ice-active surface chemically, and that the coatings were diluted enough in the droplets that were formed prior to the ice nucleation, so that freezing point depression was negligible. However, Fluka kaolinite particles, which were either coated with pure sulfuric acid or were first coated with the acid and then exposed to additional water vapor, both showed a reduced ability to nucleate ice compared to the pure particles. For the CMS kaolinite particles, the ability to nucleate ice in the immersion freezing mode was similar for all examined particles, i.e., for the pure ones and the ones with the different types of coating. Moreover, jhet derived for the CMS kaolinite particles was comparable to jhet derived for Fluka kaolinite particles coated with sulfuric acid. This is suggestive for the Fluka kaolinite possessing a type of ice-nucleating surface feature which is not present on the CMS kaolinite, and which can be destroyed by reaction with sulfuric acid. This might be potassium feldspar

    Mixture of Kosa (Asian dust) and bioaerosols detected in the atmosphere over the Kosa particles source regions with balloon-borne measurements: possibility of long-range transport

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    金沢大学フロンティアサイエンス機構Long-range transport of atmospheric microbiota with Asian dust (Kosa) particles is of great concern in Northeast Asia in view of the health effect of Kosa particles on human being, disturbance of ecosystems caused through invasion of new microbe, contribution of microorganisms to biogeochemical cycle on global/regional scales, and others. Information on atmospheric microbes over the desert areas has been desired for a long time. Detection of atmospheric microbiota on the desert regions, on the base of balloon-borne measurements, has been made at Dunhuang, China (40°00′ N, 94°30′ E; east end of Taklamakan desert) in the summer of 2007. The measurements showed that microbiota mixed internally with Kosa particles were frequently floating from the ground to about 2-km heights (above sea level), and possible long-range transport of atmospheric microbiota with dust particles taking local circulations is strongly suggested, causing active mixing of atmospheric dust over the Taklamakan desert from the ground to the free troposphere where westerly jet dominates (Iwasaka et al. in J Geophys Res 108:8652, 2003a, J Geophys Res 108:8644, b). The concentration of the mixed particles of Kosa and microbiota having a size larger than about 1 μm in diameter is estimated to be about 1 particle/cm3 at those heights on the basis of measurements of particle concentration with an optical particle counter and analysis of particles having fluorescence light due to dye of DAPI (4′6-diamidino-2 phenylindole) with an epifluorescence microscope. The mixing situation of microbiota and Kosa particles is the important factor controlling atmospheric lifetime of floating microbiota, since the mixing state certainly can protect microbiota from stressful environments [dryness, solar ultraviolet (UV) radiation, low temperature] in the atmosphere, and therefore, it is useful to discuss the data of the first description of microbiota in the atmosphere on the Taklamakan desert. © 2009 Springer Science+Business Media B.V

    A comprehensive characterization of ice nucleation by three different types of cellulose particles immersed in water

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    We present the laboratory results of immersion freezing efficiencies of cellulose particles at supercooled temperature (T) conditions. Three types of chemically homogeneous cellulose samples are used as surrogates that represent supermicron and submicron ice-nucleating plant structural polymers. These samples include microcrystalline cellulose (MCC), fibrous cellulose (FC) and nanocrystalline cellulose (NCC). Our immersion freezing dataset includes data from various ice nucleation measurement techniques available at 17 different institutions, including nine dry dispersion and 11 aqueous suspension techniques. With a total of 20 methods, we performed systematic accuracy and precision analysis of measurements from all 20 measurement techniques by evaluating T-binned (1 ∘C) data over a wide T range (−36 ∘C <T<−4 ∘C). Specifically, we intercompared the geometric surface area-based ice nucleation active surface site (INAS) density data derived from our measurements as a function of T, ns,geo(T). Additionally, we also compared the ns,geo(T) values and the freezing spectral slope parameter (Δlog(ns,geo)/ΔT) from our measurements to previous literature results. Results show all three cellulose materials are reasonably ice active. The freezing efficiencies of NCC samples agree reasonably well, whereas the diversity for the other two samples spans ≈ 10 ∘C. Despite given uncertainties within each instrument technique, the overall trend of the ns,geo(T) spectrum traced by the T-binned average of measurements suggests that predominantly supermicron-sized cellulose particles (MCC and FC) generally act as more efficient ice-nucleating particles (INPs) than NCC with about 1 order of magnitude higher ns,geo(T)

    Integrating laboratory and field data to quantify the immersion freezing ice nucleation activity of mineral dust particles

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    Data from both laboratory studies and atmospheric measurements are used to develop an empirical parameterization for the immersion freezing activity of natural mineral dust particles. Measurements made with the Colorado State University (CSU) continuous flow diffusion chamber (CFDC) when processing mineral dust aerosols at a nominal 105% relative humidity with respect to water (RHw) are taken as a measure of the immersion freezing nucleation activity of particles. Ice active frozen fractions vs. temperature for dusts representative of Saharan and Asian desert sources were consistent with similar measurements in atmospheric dust plumes for a limited set of comparisons available. The parameterization developed follows the form of one suggested previously for atmospheric particles of non-specific composition in quantifying ice nucleating particle concentrations as functions of temperature and the total number concentration of particles larger than 0.5 μm diameter. Such an approach does not explicitly account for surface area and time dependencies for ice nucleation, but sufficiently encapsulates the activation properties for potential use in regional and global modeling simulations, and possible application in developing remote sensing retrievals for ice nucleating particles. A calibration factor is introduced to account for the apparent underestimate (by approximately 3, on average) of the immersion freezing fraction of mineral dust particles for CSU CFDC data processed at an RHw of 105% vs. maximum fractions active at higher RHw. Instrumental factors that affect activation behavior vs. RHw in CFDC instruments remain to be fully explored in future studies. Nevertheless, the use of this calibration factor is supported by comparison to ice activation data obtained for the same aerosols from Aerosol Interactions and Dynamics of the Atmosphere (AIDA) expansion chamber cloud parcel experiments. Further comparison of the new parameterization, including calibration correction, to predictions of the immersion freezing surface active site density parameterization for mineral dust particles, developed separately from AIDA experimental data alone, shows excellent agreement for data collected in a descent through a Saharan aerosol layer. These studies support the utility of laboratory measurements to obtain atmospherically relevant data on the ice nucleation properties of dust and other particle types, and suggest the suitability of considering all mineral dust as a single type of ice nucleating particle as a useful first-order approximation in numerical modeling investigations

    The Ny-Ålesund Aerosol Cloud Experiment (NASCENT): Overview and First Results

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    The Arctic is warming at more than twice the rate of the global average. This warming is influenced by clouds, which modulate the solar and terrestrial radiative fluxes and, thus, determine the surface energy budget. However, the interactions among clouds, aerosols, and radiative fluxes in the Arctic are still poorly understood. To address these uncertainties, the Ny-Ålesund Aerosol Cloud Experiment (NASCENT) study was conducted from September 2019 to August 2020 in Ny-Ålesund, Svalbard. The campaign’s primary goal was to elucidate the life cycle of aerosols in the Arctic and to determine how they modulate cloud properties throughout the year. In situ and remote sensing observations were taken on the ground at sea level, at a mountaintop station, and with a tethered balloon system. An overview of the meteorological and the main aerosol seasonality encountered during the NASCENT year is introduced, followed by a presentation of first scientific highlights. In particular, we present new findings on aerosol physicochemical and molecular properties. Further, the role of cloud droplet activation and ice crystal nucleation in the formation and persistence of mixed-phase clouds, and the occurrence of secondary ice processes, are discussed and compared to the representation of cloud processes within the regional Weather Research and Forecasting Model. The paper concludes with research questions that are to be addressed in upcoming NASCENT publications

    Climate warming and decreasing total column ozone over the Tibetan Plateau during winter and spring

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    The long-term trends of the total column ozone (TCO) over the Tibetan Plateau (TP) and factors responsible for the trends are analysed in this study using various observations and a chemistry–climate model (CCM). The results indicate that the total column ozone low (TOL) over the TP during winter and spring is deepening over the recent decade, which is opposite to the recovery signal in annual mean TCO over the TP after mid-1990s. The TOL intensity is increasing at a rate of 1.4 DU/decade and the TOL area is extending with 50,000 km2/decade during winter for the period 1979–2009. The enhanced transport of ozone-poor air into the stratosphere and elevated tropopause due to the rapid and significant warming over the TP during winter reduce ozone concentrations in the upper troposphere and lower stratosphere and hence lead to the deepening of the TOL. Based on the analysis of the multiple regression model, the thermal dynamical processes associated with the TP warming accounts for more than 50% of TCO decline during winter for the period 1979–2009. The solar variations during 1995–2009 further enlarge ozone decreases over the TP in the past decade. According to the CCM simulations, the increases in NOx emissions in East Asia and global tropospheric N2O mixing ratio for the period 1979–2009 contribute to no more than 20% reductions in TCO during this period
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