Why Soot is not Alike Soot: A Molecular/Nanostructural Approach to Low Temperature Soot Oxidation

Due to worldwide increasingly sharpened emission regulations, the development of Gasoline Direct Injection and Diesel Direct Injection engines not only aims at the reduction of the emission of nitrogen oxides but also at the reduction of particulate emissions. Regarding present regulations, both tasks can be achieved solely with the help of exhaust after treatment systems. For the reduction of the emission of particulates, Gasoline (GPF) and diesel Particulate Filters (DPF) offer a solution and their implementation is intensely promoted. Under optimal conditions particulates retained on particulate filters are continuously oxidized with the exhaust residual oxygen so that the particulate filter (PF) is regenerated possibly without any additional intervention into the engine operating parameters. The regeneration behavior of PF depends on the reaction rates of soot particles with oxidative reactants at exhaust gas temperatures. The reaction rates of soot particles from internal combustion engines (ICE) often are discussed in terms of order/disorder on the particle nanoscale, the concentration and kind of functional groups on the particle surfaces, and the content of (mostly polycyclic aromatic) hydrocarbons in the soot. In this work the reactivity of different kinds of soot (soot from flames, soot from ICE, carbon black) under oxidation conditions representative for PF regeneration is investigated. Soot reactivity is determined in dynamic Temperature Programmed Oxidation (TPO) experiments and the soot primary particle morphology and nanostructure is investigated by High-Resolution Transmission Electron Microscopy (HRTEM). An image analysis method based on known methods from the literature and improving some infirmities is used to evaluate morphology and nanostructural characteristics. From this, primary particle size distributions, length and separation distance distributions as well as tortuosities of fringes within the primary particle structures are obtained. Further, UV–visible spectroscopy and Raman scattering and other diagnostic techniques are used to study the properties connected to the reactivity of soot and to corroborate the experimental findings. It is found that nanostructural characteristics predominantly affect reactivity. Oxidation rates are derived from TPO and interpreted on a molecular basis from quantum chemistry calculations revealing a replication/activation oxidation mechanism

Numerical evaluation of a novel double-concentric swirl burner for sulfur combustion

A burner system for the efficient and clean combustion of sulfur is introduced, which serves as a key component in a novel solar power cycle using sulfur as chemical storage medium of solar energy. In order to validate the proposed design concept, highly-resolved numerical simulations have been performed. The current setup is operated with a thermal load of 20 kW or power density of 5 MW/m$^{3}$. Two nozzle configurations with different swirl intensities (SI) of the airflow are studied. A large inner recirculation zone is observed for the nozzle with a high SI (HSI), which leads to a strong radial dispersion of the sulfur spray and a broad, short flame in the combustion chamber; although this HSI design is beneficial from the viewpoint of flame stabilization, it causes a large number of sulfur droplets hitting the chamber wall. In contrast, the nozzle design with a low SI (LSI) yields a narrow spray and a long jet flame, with much less droplets hitting the wall. The HSI nozzle shows an overall higher flame temperature compared with the LSI nozzle, which is confirmed to be caused by burning at a higher local fuel equivalence ratio. This is attributed to the strong inner recirculation flow generated by the high swirl intensity, which results in an enhanced evaporation and mixing of sulfur droplets with air. In terms of operability and NOx emission, the LSI burner is preferred due to less sulfur droplets hitting the chamber wall and the lower flame temperature

(Z)-2-benzylidene-2H-[1, 4] benzothiazin-3-one(T1) as New Synthesized Corrosion Inhibitor for Mild Steel in 0.5 M H2SO4

The corrosion inhibition of mild steel in 0.5 M H2SO4 solution by (Z)-2-benzylidene-2H-[1,4]benzothiazin-3-one: (T1)  has been studied using electrochemical polarization , electrochemical impedance spectroscopy (EIS) and weight loss methods. The corrosion inhibition efficiency measured by all the three techniques was in good agreement with each other. The results showed that T1 is a very good inhibitor for mild steel in acidic media. The inhibition efficiency increases with increasing inhibitor concentration. It acts as a mixed-type inhibitor. EIS plots indicated that the addition of T1 increases the charge-transfer resistance (Rct), decreases the double-layer capacitance (Cdl) of the corrosion process, and hence increases inhibition efficiency. The adsorption of the T1 on the mild steel surface in acid solution obeys the Langmuir adsorption isotherm

Toric Calabi-Yau supermanifolds and mirror symmetry

We study mirror symmetry of supermanifolds constructed as fermionic extensions of compact toric varieties. We mainly discuss the case where the linear sigma A-model contains as many fermionic fields as there are U(1) factors in the gauge group. In the mirror super-Landau-Ginzburg B-model, focus is on the bosonic structure obtained after integrating out all the fermions. Our key observation is that there is a relation between the super-Calabi-Yau conditions of the A-model and quasi-homogeneity of the B-model, and that the degree of the associated superpotential in the B-model is given in terms of the determinant of the fermion charge matrix of the A-model.Comment: 20 pages, v2: references adde