Evaluation of potential radiological hazards of unfired construction materials containing fly ash in Vietnam.

In this study, the specific activities of 226Ra, 232Th and 40K in the unfired construction materials (solid card bricks, 4-hole bricks, pavement bricks) containing fly ash and bottom ash from a coal-fired thermal power plant in Vietnam were measured using the low-level gamma-ray spectrometer with HPGe detector. Also, the 222Rn concentrations in these materials were analyzed using RAD7 radon monitor and then radon mass exhalation rate and emanation fraction of these materials were calculated. The potential radiological hazards for residents living in the model room made of these materials were evaluated. The average specific activity of 226Ra, 232Th and 40K were found as 67.7, 79.3 and 703.5 Bq kg-1, respectively. The total annual effective dose (due to external gamma exposure and internal radon exposure for resident living in the CEN model room made of the unfired brick samples) was found as 0.9 mSv y-1 which is lower than the worldwide average dose of 2.4 mSv y-1. Calculations from ResRad-Build code showed that the doses due to radon exposure account for from 62.3% (at the first year) to 98.8% (at the next 30 years) of the total gamma and radon dose. Under low air exchange to the outside environment, from the 6th year onwards, the total dose may exceed the average dose value from natural radiation exposure sources.

Hydroxyapatite Derived from Salmon Bone As Green Ecoefficient Support for Ceria-Doped Nickel Catalyst for CO2 Methanation.

Hydroxyapatite (HA) derived from salmon bone byproducts is used as a green support for the nanostructured nickel catalysts applied in the methanation of carbon dioxide (CO2). Undoped nickel catalysts and various ceria-doped nickel supported on hydroxyapatite (HA) were prepared by coimpregnation. Characteristics of the as-prepared catalysts were investigated by the various techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET), hydrogen temperature-programmed reduction (H2-TPR), carbon dioxide temperature-programmed desorption (CO2-TPD), and energy-dispersive X-ray spectroscopy (EDX). The catalyst activity was assessed throughout CO2 methanation in the low-temperature range of 225-350 °C with the molar ratio of H2/CO2 = 4/1. The function of HA and ceria provided a high dispersity of nickel particles over the catalyst surface with the size range of 24.5-25.8 nm, leading to improvement in the reduction and CO2 adsorption capacity of the catalysts as well as enhancing the catalytic efficiency in CO2 methanation. The 10Ni/HA catalyst reduced at suitable conditions of 400 °C for 2 h showed the highest catalytic performance among the tested catalysts. CO2 conversion and CH4 selectivity reached 76.6 and 100% at a reaction temperature of 350 °C, respectively. The results show that the Ni/HA sample doped with 6.0 wt % ceria was the best, with the CO2 conversion and the CH4 selectivity reaching 92.5% and 100%, respectively, at a reaction temperature of 325 °C.

Synthesis, Characteristics, Oil Adsorption, and Thermal Insulation Performance of Cellulosic Aerogel Derived from Water Hyacinth.

Cellulosic aerogel from water hyacinth (WH) was synthesized to address the dual environmental issues of water hyacinth pollution and the production of a green material. Raw WH was treated with sodium hydroxide (NaOH) with microwave assistance and in combination with hydrogen peroxide (H2O2). The results from X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, and scanning electron microscopy (SEM) showed that lignin and hemicellulose were markedly decreased after treatment, reducing from 24.02% hemicellulose and 5.67% lignin in raw WH to 8.32 and 1.92%, respectively. Cellulose aerogel from the pretreated WH had a high porosity of 98.8% with a density of 0.0162 g·cm-3 and a low thermal conductivity of 0.030 W·m-1·K-1. After modification with methyl trimethoxysilane (MTMS) to produce a highly hydrophobic material, WH aerogel exhibited high stability for oil absorption at a capacity of 43.3, 43.15, 40.40, and 41.88 (g·g-1) with diesel oil (DO), motor oil (MO), and their mixture with water (DO + W and MO + W), respectively. The adsorption remained stable after 10 cycles.