scholarly journals Volatilized and Condensed Sb- and As-Bearing Phases Produced During Roasting of Cu-Rich Complex Concentrate in Nitrogen Atmosphere with Oxygen in Traces

Author(s):  
Pande Nishant Prasad ◽  
Andreas Lennartsson ◽  
Caisa Samuelsson

AbstractA Cu-rich complex sulpfide concentrate (containing Sb as sulphosalts and gudmundite, and As as arsenopyrite) is roasted in Nitrogen atmosphere carrying traces of oxygen ($${\text{p}}^{{\text{O}}_{2}} \approx {10}^{-5.3}\text{ bar)}$$ p O 2 ≈ 10 - 5.3 bar) . In situ measurements through QMS indicated that the volatilized species are mainly elemental sulfur, S2(g), and gaseous sulfur oxides. Sb- and As-bearing volatilized species could not be detected, owing to their low concentrations in the gas phase. Characterization studies through XRD and SEM-EDS confirmed that the condensates collected at room temperature during the roasting experiments comprised of (1) cyclo-octa sulfur, S8(s) and polysulfur oxides, Sn−xOx(s); (2) amorphous trisulfides of Sb and As; (3) and cubic crystalline trioxides of Sb and As. The solid phases in the condensate were found to be fine-sized (sub-micronic) and widely intermixed. Consequently, quantification of the solid phases in the condensates through direct measurement techniques like QEMSCAN was not possible. A novel approach of partial quantification of solid phases in the condensate through a stochastic model-based calculation approach is also presented. The model results suggested the occurrence of vapor-phase complexation of sulfides of Sb and As in the gas phase. Additional attributes of the volatilized species could be determined through a thermodynamic equilibrium calculation showing that the formation of the complex oxides, As4−nSbnO6(g), would be negligible compared to that of the complex sulfides, As4−nSbnS6(g).

2014 ◽  
Vol 7 (6) ◽  
pp. 1571-1580 ◽  
Author(s):  
J. Kaiser ◽  
X. Li ◽  
R. Tillmann ◽  
I. Acir ◽  
F. Holland ◽  
...  

Abstract. Two gas-phase formaldehyde (HCHO) measurement techniques, a modified commercial wet-chemical instrument based on Hantzsch fluorimetry and a custom-built instrument based on fiber laser-induced fluorescence (FILIF), were deployed at the atmospheric simulation chamber SAPHIR (Simulation of Atmospheric PHotochemistry In a large Reaction Chamber) to compare the instruments' performances under a range of conditions. Thermolysis of para-HCHO and ozonolysis of 1-butene were used as HCHO sources, allowing for calculations of theoretical HCHO mixing ratios. Calculated HCHO mixing ratios are compared to measurements, and the two measurements are also compared. Experiments were repeated under dry and humid conditions (RH < 2% and RH > 60%) to investigate the possibility of a water artifact in the FILIF measurements. The ozonolysis of 1-butene also allowed for the investigation of an ozone artifact seen in some Hantzsch measurements in previous intercomparisons. Results show that under all conditions the two techniques are well correlated (R2 ≥ 0.997), and linear regression statistics show measurements agree with within stated uncertainty (15% FILIF + 5% Hantzsch). No water or ozone artifacts are identified. While a slight curvature is observed in some Hantzsch vs. FILIF regressions, the potential for variable instrument sensitivity cannot be attributed to a single instrument at this time. Measurements at low concentrations highlight the need for a secondary method for testing the purity of air used in instrument zeroing and the need for further FILIF White cell outgassing experiments.


2007 ◽  
Vol 85 (2) ◽  
pp. 96-104 ◽  
Author(s):  
T Stanley Cameron ◽  
Andreas Decken ◽  
Mary Gabriel ◽  
Carsten Knapp ◽  
Jack Passmore

The stepwise symmetry-allowed cycloaddition reactions of [SNS]+ with the dinitriles NC–X–CN (X = CCl2, CO) were investigated. The reaction of [SNS]+ and dinitrile in 2:1 ratio yielded the dicycloaddition product quantitatively after 2 weeks (in situ 13C NMR). At a 1:1 ratio, mixtures of mono- and dicycloaddition products were obtained that could not be completely separated from one another. The energetics of the reaction were estimated in the gas phase, in solution (SO2 and CH2Cl2), and solid phases using DFT calculations (PBE0/6-311G*) and a "volume-based thermodynamics" approach for lattice enthalpies. Monocycloaddition products are stable in the gas phase and in solution with respect to disproportionation reactions, but in the solid state the disproportionation of 2 [NC–X–(CNSNS)][AsF6] into [X(CNSNS)2][AsF6]2 and NC–X–CN is strongly favored because of the higher lattice enthalpy of the 1:2 salt. In the gas phase, the second cycloaddition is endothermic because of the charge repulsion of the two positive charges, but in the solid state the reaction is strongly favored because of the lattice enthalpy gain on the formation of the 1:2 ([X(CNSNS)2][AsF6]2) from two 1:1 salts ([NC–X–(CNSNS)][AsF6] and [SNS][MF6]). The crystal structures of the dicycloaddition products [Cl2C(CNSNS)2][AsF6]2 and [OC(CNSNS)2][AsF6]2 and the monocycloaddition product [Cl2C(CNSNS)CN][AsF6] were obtained. In [Cl2C(CNSNS)CN][AsF6], the free nitrile groups interact with neighboring heterocycles further demonstrating that potential of free nitrile groups for introducing intermolecular interactions. [OC(CNSNS)2]2+ is a planar dication, which adopts the conformation with Sδ+···Oδ– contacts to optimize intramolecular electrostatic interactions.Key words: crystal structure, sulfur-nitrogen, 1,3,2,4-dithiadiazolyium, nitriles, cycloaddition, DFT calculations, thermodynamics, energetics.


Energy ◽  
2021 ◽  
Vol 216 ◽  
pp. 119227
Author(s):  
Yan Ding ◽  
Yunchao Li ◽  
Yujie Dai ◽  
Xinhong Han ◽  
Bo Xing ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 163
Author(s):  
Iryna Zelenina ◽  
Igor Veremchuk ◽  
Yuri Grin ◽  
Paul Simon

Nano-scaled thermoelectric materials attract significant interest due to their improved physical properties as compared to bulk materials. Well-shaped nanoparticles such as nano-bars and nano-cubes were observed in the known thermoelectric material PbTe. Their extended two-dimensional nano-layer arrangements form directly in situ through electron-beam treatment in the transmission electron microscope. The experiments show the atomistic depletion mechanism of the initial crystal and the recrystallization of PbTe nanoparticles out of the microparticles due to the local atomic-scale transport via the gas phase beyond a threshold current density of the beam.


2021 ◽  
Vol 13 (7) ◽  
pp. 1238
Author(s):  
Jere Kaivosoja ◽  
Juho Hautsalo ◽  
Jaakko Heikkinen ◽  
Lea Hiltunen ◽  
Pentti Ruuttunen ◽  
...  

The development of UAV (unmanned aerial vehicle) imaging technologies for precision farming applications is rapid, and new studies are published frequently. In cases where measurements are based on aerial imaging, there is the need to have ground truth or reference data in order to develop reliable applications. However, in several precision farming use cases such as pests, weeds, and diseases detection, the reference data can be subjective or relatively difficult to capture. Furthermore, the collection of reference data is usually laborious and time consuming. It also appears that it is difficult to develop generalisable solutions for these areas. This review studies previous research related to pests, weeds, and diseases detection and mapping using UAV imaging in the precision farming context, underpinning the applied reference measurement techniques. The majority of the reviewed studies utilised subjective visual observations of UAV images, and only a few applied in situ measurements. The conclusion of the review is that there is a lack of quantitative and repeatable reference data measurement solutions in the areas of mapping pests, weeds, and diseases. In addition, the results that the studies present should be reflected in the applied references. An option in the future approach could be the use of synthetic data as reference.


Polymers ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 1900
Author(s):  
Ramin Hosseinnezhad ◽  
Iurii Vozniak ◽  
Fahmi Zaïri

The paper discusses the possibility of using in situ generated hybrid polymer-polymer nanocomposites as polymeric materials with triple shape memory, which, unlike conventional polymer blends with triple shape memory, are characterized by fully separated phase transition temperatures and strongest bonding between the polymer blends phase interfaces which are critical to the shape fixing and recovery. This was demonstrated using the three-component system polylactide/polybutylene adipateterephthalate/cellulose nanofibers (PLA/PBAT/CNFs). The role of in situ generated PBAT nanofibers and CNFs in the formation of efficient physical crosslinks at PLA-PBAT, PLA-CNF and PBAT-CNF interfaces and the effect of CNFs on the PBAT fibrillation and crystallization processes were elucidated. The in situ generated composites showed drastically higher values of strain recovery ratios, strain fixity ratios, faster recovery rate and better mechanical properties compared to the blend.


Processes ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 965
Author(s):  
Zoé Perrin ◽  
Nathalie Carrasco ◽  
Audrey Chatain ◽  
Lora Jovanovic ◽  
Ludovic Vettier ◽  
...  

Titan’s haze is strongly suspected to be an HCN-derived polymer, but despite the first in situ measurements by the ESA-Huygens space probe, its chemical composition and formation process remain largely unknown. To investigate this question, we simulated the atmospheric haze formation process, experimentally. We synthesized analogues of Titan’s haze, named Titan tholins, in an irradiated N2–CH4 gas mixture, mimicking Titan’s upper atmosphere chemistry. HCN was monitored in situ in the gas phase simultaneously with the formation and evolution of the haze particles. We show that HCN is produced as long as the particles are absent, and is then progressively consumed when the particles appear and grow. This work highlights HCN as an effective precursor of Titan’s haze and confirms the HCN-derived polymer nature of the haze.


Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1667
Author(s):  
Mikhail Karushev

Fast and reversible cobalt-centered redox reactions in metallopolymers are the key to using these materials in energy storage, electrocatalytic, and sensing applications. Metal-centered electrochemical activity can be enhanced via redox matching of the conjugated organic backbone and cobalt centers. In this study, we present a novel approach to redox matching via modification of the cobalt coordination site: a conductive electrochemically active polymer was electro-synthesized from [Co(Amben)] complex (Amben = N,N′-bis(o-aminobenzylidene)ethylenediamine) for the first time. The poly-[Co(Amben)] films were investigated by cyclic voltammetry, electrochemical quartz crystal microbalance (EQCM), in situ UV‑vis-NIR spectroelectrochemistry, and in situ conductance measurements between −0.9 and 1.3 V vs. Ag/Ag+. The polymer displayed multistep redox processes involving reversible transfer of the total of 1.25 electrons per repeat unit. The findings indicate consecutive formation of three redox states during reversible electrochemical oxidation of the polymer film, which were identified as benzidine radical cations, Co(III) ions, and benzidine di-cations. The Co(II)/Co(III) redox switching is retained in the thick polymer films because it occurs at potentials of high polymer conductivity due to the optimum redox matching of the Co(II)/Co(III) redox pair with the organic conjugated backbone. It makes poly-[Co(Amben)] suitable for various practical applications based on cobalt-mediated redox reactions.


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