Toward On-Line Slag Composition Analysis: Optical Emissions from Laboratory Electric Arc

We acknowledge the support of Research Fund for Coal and Steel under grant agreement No. 709923, Academy of Finland for Genome of Steel grant No. 311934, Business Finland for Grant No. 4478/31/2019, Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART2.Electric arc furnaces and ladle furnaces have an important role in the future of steelmaking where CO 2 emissions have to be mitigated to an acceptable level. One way to address this goal is to optimize and improve the current practices by adjusting the chemistry and reactions with material additions or gas injections. These procedures would greatly benefit from on-line slag composition analysis. Since the electric arcs radiate throughout the melting, optical emission spectroscopy is a potential method for such analysis. In this study, optical emissions from the electric arc are measured in a laboratory environment. Dozens of atomic emission lines were correlated with Cr 2O 3, Fe 2O 3, Al 2O 3, SiO 2, MnO, MgO, CaO, CaF 2, V 2O 5, and Ni content of the slag together with correlation between CaF 2 and molecular optical emission bands of CaF. Optimal spectral resolution for industrial applications was deducted to be between 0.022 and 0.179 nm. © 2021, The Author(s). --//-- Published under the CC BY license.Academy of Finland for Genome of Steel 311934, 4478/31/2019; Research Fund for Coal and Steel 709923; Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART2

Vacuum ultraviolet excitation luminescence spectroscopy of few-layered MoS 2

We report on vacuum ultraviolet (VUV) excited photoluminescence (PL) spectra emitted from a chemical vapor deposited MoS₂ few-layered film. The excitation spectrum was recorded by monitoring intensities of PL spectra at ~1.9 eV. A strong wide excitation band peaking at 7 eV was found in the excitation. The PL excitation band is most intensive at liquid helium temperature and completely quenched at 100 K. Through first-principles calculations of photoabsorption in MoS₂, the excitation was explicated and attributed to transitions of electrons from p- and d- type states in the valence band to the d- and p-type states in the conduction band. The obtained photon-in/photon-out results clarify the excitation and emission behavior of the low dimensional MoS₂ when interacting with the VUV light sources

Deep-core photoionization of krypton atoms below and above the 1s ionization threshold

Electronic relaxation of atomic Kr below and above the 1s ionization threshold is investigated experimentally using hard x-ray photoelectron spectroscopy. The experimental results are interpreted with the aid of relativistic Dirac-Fock calculations. The 1s orbital core-hole lifetime is extracted and the satellite's structures accompanying the photoelectron main line are assigned. Auger spectra recorded below and above the K edge are also investigated. In particular, the Auger cascade originating from vacancies of different origin in the L shell is analyzed in great detail. Competition between radiative KL versus nonradiative KLL Auger emission is emphasized

Valence electronic structure and photofragmentation of 1,1,1,2-tetrafluoroethane (CF3-CH2F)

The electronic structure and fragmentation of the hydrofluorocarbon compound 1,1,1,2-tetrafluoroethane (CF3-CH2F) were studied using spectroscopical methods and quantum chemical calculations. Valence photoelectron spectra and the ionic fragmentation products were recorded with synchrotron radiation in the vacuum ultraviolet (VUV) region. The geometric and electronic structures of the CF3-CH2F molecule were calculated using the complete active space perturbation theory of second order. The calculated vertical ionization energies were used to interpret the experimental photoelectron spectrum. VUV photodissociation of the sample molecule was studied with photoelectron-photoion coincidence spectroscopy. Coincident ion yields are shown for several cations as a function of electron binding energy. The experimental data are discussed in comparison with theory and previous work

Towards designing reactive glasses for alkali activation : understanding the origins of alkaline reactivity of Na-Mg aluminosilicate glasses

Alkali-activated materials (AAMs), sometimes called geopolymers, are eco-friendly cementitious materials with reduced carbon emissions when compared to ordinary Portland cement. However, the availability of most precursors used for AAM production may decline in the future because of changes in industrial sectors. Thus, new precursors must be developed. Recently there has been increased interest in synthetic glass precursors. One major concern with using synthetic glasses is ensuring that they react sufficiently under alkaline conditions. Reactivity is a necessary, although not sufficient, requirement for a suitable precursor for AAMs. This work involves the synthesis, characterization, and estimation of alkaline reactivity of Na-Mg aluminosilicate glasses. Structural characterization showed that replacing Na with Mg led to more depolymerization. Alkaline reactivity studies indicated that, as Mg replaced Na, reactivity of glasses increased at first, reached an optimal value, and then declined. This trend in reactivity could not be explained by the conventional parameters used for estimating glass reactivity: the non-bridging oxygen fraction (which predicts similar reactivity for all glasses) and optical basicity (which predicts a decrease in reactivity with an increase in Mg replacement). The reactivity of the studied glasses was found to depend on two main factors: depolymerization (as indicated by structural characterization) and optical basicity. Depolymerization dominated initially, which led to an increase in reactivity, while the effect of optical basicity dominated later, leading to a decrease in reactivity. Hence, while designing reactive synthetic glasses for alkali activation, structural study of glasses should be given due consideration in addition to the conventional factors

Evidence of formation of an amorphous magnesium silicate (AMS) phase during alkali activation of (Na-Mg) aluminosilicate glasses

There is some ambiguity regarding the fate of Mg during the alkali activation of Mg-rich precursors within the broader field of alkali activated materials (AAMs). The present work addresses this issue by studying the reaction products in AAMs synthesized from (Na-Mg) aluminosilicate glasses. Here, instead of magnesium silicate hydrate (M-S-H) phase, Mg exclusively forms an amorphous magnesium silicate (AMS) phase. Compared to M-S-H, AMS is a more depolymerized phase, which has not previously been well documented. The formation of AMS seems to be driven by the high charge density of the Mg cation which effectively stabilizes the depolymerized silicate species. We also show that the lack of hydrotalcite-group phases is due to aluminum depletion by zeolite formation. This work highlights the need to consider the existence of the AMS phase in Mg-containing AAMs, especially in complex systems, where its identification may be difficult

Performance and characterization of the FinEsuseAMS beamline at the MAX IV Laboratory

FinEstBeAMS (Finnish-Estonian Beamline for Atmospheric and Materials Sciences) is a multidisciplinary beamline constructed at the 1.5 GeV storage ring of the MAX IV synchrotron facility in Lund, Sweden. The beamline covers an extremely wide photon energy range, 4.5-1300 eV, by utilizing a single elliptically polarizing undulator as a radiation source and a single grazingincidence plane grating monochromator to disperse the radiation. At photon energies below 70 eV the beamline operation relies on the use of optical and thin-film filters to remove higher-order components from the monochromated radiation. This paper discusses the performance of the beamline, examining such characteristics as the quality of the gratings, photon energy calibration, photon energy resolution, available photon flux, polarization quality and focal spot size

Trophic structure of Lake Tanganyika: Carbon flows in the pelagic food web

peer reviewedThe sources of carbon for the pelagic fish production in Lake Tanganyika, East Africa, were evaluated in a comprehensive multi-year study. Phytoplankton production was assessed from seasonal in situ 14C and simulated in situ results, using on-board incubator measurements and knowledge of the vertical distributions of chlorophyll and irradiance. Bacterioplankton production was measured on two cruises with the leucine incorporation method. Zooplankton production was calculated from seasonal population samples, the carbon contents of different developmental stages and growth rates derived from published sources. Fish production estimates were based on hydroacoustic assessment of pelagic fish biomass and data on growth rates obtained from length frequency analyses and checked against daily increment rings of fish otoliths. Estimates for primary production (426-662 g C m-2 a-1) were 47-128% higher than previously published values. Bacterioplankton production amounted to about 20% of the primary production. Zooplankton biomass (1 g C m-2) and production (23 g C m-2 a-1) were 50% lower than earlier reported, suggesting that the carbon transfer efficiency from phytoplankton to zooplankton was low, in contrast to earlier speculations. Planktivorous fish biomass (0.4 g C m-2) and production (1.4-1.7 g C m-2 a-1) likewise indicated a low carbon transfer efficiency from zooplankton into planktivorous fish production. Relatively low transfer efficiencies are not unexpected in a deep tropical lake, because of the generally high metabolic losses due to the high temperatures and presumably high costs of predator avoidance. The total fisheries yield in Lake Tanganyika in the mid- 1990s was 0.08-0.14% of pelagic primary production, i.e. within the range of typical values in lakes. Thus, no special mechanisms need be invoked to explain the productivity of fisheries in Lake Tanganyika