Hydrogen peroxide (H2O2), an oxidizer produced by water radiolysis, is considered one of the main contributors to corrosion of the stainless steel (SS) components in the cooling system of nuclear reactors. The detailed understanding of this chemical system is however still missing. The present research aimed to study the effects of H2O2 on 304 SS. The surface morphology and the chemical composition of the SS specimens after experiment were examined using Scanning Electron Microscope – Energy Dispersive X-ray (SEM-EDX). The change in atomic % of Fe, Cr, Ni, and O as a function of temperature will be reported. The corrosion type and possible corrosion products will be proposed and discussed.
Zinc injection has been widely applied in nuclear industry for corrosion mitigation of nuclear materials. The corrosion resistance mechanism of zinc in the presence of the radiolytic oxidizing species is complex and has not been completely understood. Without such information it is not possible to improve the protocol. In the present study, zinc effects on corrosion of 304 SS exposed to H2O2 at 200-1000 ppb for 7 and 70 hrs were investigated at room temperature using a custom-made flow setup. XRF and SEM-EDX were used to examine the chemical composition and surface morphology of the specimens. The results indicated that pitting was the dominant form of corrosion found under the experimental conditions. Zinc ions tend to help mitigate corrosion of the material via playing a significant role in oxide formation on the steel surface.
Generally, it is difficult to generate a high-performance pure blue emission organic light-emitting diode (OLED). That is because the intrinsically wide band-gap makes it hard to inject charges into the emitting layer in such devices. To solve the problem, carbazole derivatives have been widely used because they have more thermal stability, a good hole transporting property, more electron rich (p-type) material, and higher photoconductivity. In the present work, novel copolymers containing donor-acceptor-acceptor-donor (D-A-A-D) blue compounds used for OLEDs were investigated. The theory of the geometrical and electronic properties of N-ethylcarbazole (ECz) as donor molecule (D) coupled to a series of 6 acceptor molecules (A) for advanced OLEDs were investigated. The acceptors were thiazole (TZ), thiadiazole (TD), thienopyrazine (TPZ), thienothiadiazole (TTD), benzothiadiazole (BTD), and thiadiazolothienopyrazine (TDTP). The ground state structure of the copolymers were studied using Density Functional Theory (DFT) at B3LYP/6-31G(d) level. Molecular orbital analysis study indicated 3 investigated copolymers (ECz-diTZ-ECz, ECz-diTD-ECz, ECz-diBTD-ECz) have efficient bipolar charge transport properties for both electron and hole injection to the TiO2 conduction band (4.8 eV). In addition, the excited states electronic properties were calculated using Time-Dependent Density Functional Theory (TD-DFT) at the same level. Among these investigated copolymer ECz-diTZ-ECz and ECz-diTD-ECz showed the maximum absorption wavelengths (λabs) with blue emitting at 429 and 431 nm, respectively. The results suggested that selected D-A-A-D copolymers can improve the electron- and hole- transporting abilities of the devices. Therefore, the designed copolymers would be a promising material for future development of light-emitting diodes, electrochromic windows, photovoltaic cells, and photorefractive materials.
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