a b s t r a c tThe activity concentration of 226 Ra, 232 Th and 40 K was measured in commonly building materials used in Nigeria from commercial supplier using High Purity Germanium Gamma (HPGe) detector. The mean activity concentrations in the samples were found to be 51.5 ± 9.3, 72.46 ± 17.65 and 217.05 ± 44.31 Bqkg À1 for 226 Ra, 232 Th and 40 K respectively. The highest radium equivalent (Ra eq ) of 273.9 Bqkg À1 was noted in Perfect Superfix White Cement (Nigeria) but found to be < 370 Bqkg À1 as the recommended dose limiting safe value for bulk media as presumed, the highest value of internal hazard index (H in ) and external hazard index (H ex ) of 0.894 and 0.744 respectively were also < 1. The absorbed dose rate (DR) with a value of 122.52 nGyh À1 noted in ceramic tile sample is higher than the weighted population world average value of 80 nGyh À1 by a factor of 1.53. The highest annual effective dose rate (AEDR) of 0.601 mSvy À1 reported in PNT ceramics but was found to be less < 1 mSvy À1 . The investigated materials have the values of H in , H ex and AEDR greater than 0.5 but less than1, showing that the dose impact exceeds the exemption dose level of 0.3 mSvy À1 for AEDR but complies to the upper limit of dose principle of 1 mSvy À1 .
In this investigation, natural radioactive contents in tiles manufactured in Nigeria and tiles imported from China were measured using gamma ray spectroscopy. High Purity Germanium detector was used to estimate the concentrations of some radioisotopes present in 17 samples of various tiles from Nigeria and China. The average activity concentrations of 226Ra, 232Th, and 40K for the tiles were found to be 68.2 ± 0.5; 173.9 ± 9.2 and 490 ± 15 Bq/kg and 58.2 ± 0.5, 161.5 ± 9.4 and 455.7 ± 15.1 Bq/kg for the tiles from Nigeria and China respectively. Radiological hazard indices such as absorbed dose rate, radium equivalent activity, external Hazard Index (Hex), internal Hazard Index (Hin), Annual Effective Dose (mSv/y), Gamma activity Index (Iγ) and Alpha Index (Iα) were determined for both kind of tiles from Nigeria and China. The mean values obtained were: 354.56 and 317.16 Bq/kg; 169.22 nGyh−1 and 153.92 nGyh−1; 0.95 and 0.87; 1.14 and 1.08; 1.59 mSv/y and 1.52 mSv/y; 1 and 1.15 and; 0.34 and 0.29 respectively. The mean value of radium equivalent obtained in this study is less than that of the international reference value of 370 Bq/kg for the both kind of tiles.
Lithium-
and manganese-rich transition-metal oxide (LMR-NMC) electrodes have been designed either
as heterostructures of the primary components (“composite”)
or as core–shell structures with improved electrochemistry
reported for both configurations when compared with their primary
components. A detailed electrochemical and structural investigation
of the 0.5Li2MnO3–0.5LiNi0.5Mn0.3Co0.2O2 composite and core–shell
structured positive electrode materials is reported. The core–shell
material shows better overall electrochemical performance compared
to its corresponding composite material. While both configurations
gave the same initial charge capacity of ∼300 mAh/g when cycled
at a rate of 10 mA/g at 25 °C, the core–shell sample gives
a discharge capacity of 232 mAh/g compared to 208 mAh/g delivered
by the composite sample. Also, the core–shell sample gave better
rate capability and a smaller first-cycle irreversible capacity loss
than the composite sample. The improved performance of the core–shell
material is attributed to its lower surface reactivity and limited
structural change since the more stable Li2MnO3 shell screens the more reactive Ni-rich core material from interacting
with either air or electrolyte at high potentials, thereby preventing
electrode surface modification. In situ X-ray diffraction correlated
with electrochemical data revealed that the composite sample shows
stronger volumetric changes in the lattice parameters during charging
to 4.8 V. In addition, X-ray absorption spectroscopy showed an incomplete
Ni reduction process after the first discharge for the composite sample.
From these results, it was shown that this leads to a more severe
degradation in the composite material that affects Li+ intercalation
in the subsequent discharge, thereby resulting in its poorer performance.
Furthermore, to confirm these results, another LMR-NMC material with
a different composition (having a Ni-poor core)0.5Li2MnO3-0.5LiNi0.33Mn0.33Co0.33O2was investigated. The core–shell structured
positive electrode material also gave an improved electrochemical
performance compared to the corresponding composite positive electrode
material. These results show that the core–shell configuration
could effectively be used to improve the performance of the LMR-NMC
materials to enable future high-energy applications.
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