Large-Eddy Simulations of Spray a Flames Using Explicit Coupling of the Energy Equation with the FGM Database

This paper provides a numerical study on n-dodecane flames using Large-Eddy Simulations (LES) along with the Flamelet Generated Manifold (FGM) method for combustion modeling. The computational setup follows the Engine Combustion Network Spray A operating condition, which consists of a single-hole spray injection into a constant volume vessel. Herein we propose a novel approach for the coupling of the energy equation with the FGM database for spray combustion simulations. Namely, the energy equation is solved in terms of the sensible enthalpy, while the heat of combustion is calculated from the FGM database. This approach decreases the computational cost of the simulation because it does not require a precise computation of the entire composition of the mixture. The flamelet database is generated by simulating a series of counterflow diffusion flames with two popular chemical kinetics mechanisms for n-dodecane. Further, the secondary breakup of the droplet is taken into account by a recently developed modified version of the Taylor Analogy Breakup model. The numerical results show that the proposed methodology captures accurately the main characteristics of the reacting spray, such as mixture formation, ignition delay time, and flame lift-off. Additionally, it captures the “cool flame" between the flame lift-off and the injection nozzle. Overall, the simulations show differences between the two kinetics mechanisms regarding the ignition characteristics, while similar flame structures are observed once the flame is stabilised at the lift-off distance.

     

Crystal structure of the binary complex of cobalt and zinc chlorides with carbamide [Co(OCN<Subscript>2</Subscript>H<Subscript>4</Subscript>)<Subscript>5</Subscript>(H<Subscript>2</Subscript>O)][ZnCl<Subscript>4</Subscript>]

Mixed single crystals of [Co(OCN₂H₄)₅(H₂O)][ZnCl₄] were grown by the isothermal evaporation of an aqueous solution. The crystal structure of this complex was established by X-ray diffraction (R = 0.052 based on 7003 reflections). The crystals consist of [Co(OCN₂H₄)₅(H₂O)]²⁺ cations containing Co atoms in an octahedral coordination and [ZnCl₄]²⁻] anions containing Zn atoms in a tetrahedral coordination. The carbamide molecules are involved in both intramolecular and interionic hydrogen bonds. The H₂O molecule forms hydrogen bonds with the anions.     

镍,钴与zincon的络合吸附波研究：铜精矿中微量镍,钴的同时测定

有关利用络合物的极谱催化波连续测定镍,钴的报道较少。在研究铜-Zincon的极谱行为时,我们发现NH_4Cl-Na_2SO_3(pH=6.5～7.5)底液中当Zincon浓度>4×10~(-5)·mol/L时,单扫描示波极谱仪上有两个峰,其峰电位分别为-0.42V和-0.56v(vs.     

Common Information Components Analysis

Wyner’s common information is a measure that quantifies and assesses the commonality between two random variables. Based on this, we introduce a novel two-step procedure to construct features from data, referred to as Common Information Components Analysis (CICA). The first step can be interpreted as an extraction of Wyner’s common information. The second step is a form of back-projection of the common information onto the original variables, leading to the extracted features. A free parameter γ controls the complexity of the extracted features. We establish that, in the case of Gaussian statistics, CICA precisely reduces to Canonical Correlation Analysis (CCA), where the parameter γ determines the number of CCA components that are extracted. In this sense, we establish a novel rigorous connection between information measures and CCA, and CICA is a strict generalization of the latter. It is shown that CICA has several desirable features, including a natural extension to beyond just two data sets.     

Synthesis and crystal structures of coordination compounds of pyridoxine with zinc and cadmium sulfates

The pyridoxine complexes with zinc and cadmium sulfates are synthesized. The IR absorption spectra and thermal behavior of the synthesized compounds are described. Crystals of the [M(C₈H₁₁O₃N)₂(H₂O)₂]SO₄ · 3H₂O (M = Zn, Cd) compounds are investigated using X-ray diffraction. In the structures of both compounds, the M atoms are coordinated by the oxygen atoms of the deprotonated OH group and the CH₂OH group retaining its own hydrogen atom, as well as by two H₂O molecules, and have an octahedral coordination. The nitrogen atom of the heterocycle is protonated, so that the heterocycle acquires a pyridinium character. The cationic complexes form layers separated by the anions and crystallization water molecules located in between. The structural units of the crystals are joined together by a complex system of hydrogen bonds.