Monitoring of 137Cs, 239+240Pu, and 90Sr in the marine environment of South Korea and their impact on marine biota: 10 years after the Fukushima accident.

This study conducted an analysis of the behavior of radionuclides and assessment their radioactive risk based on seawater and seabed sediment samples gathered from the East, South, and Yellow Seas of South Korea over the period from 2011 to 2020. The distribution for each radionuclides in seawater obtained from the East, South, and Yellow Seas were similar. However, the concentrations of 137Cs and 239+240Pu in sediments from the East Sea were observed to be higher compared to those from the South and Yellow Seas. This variation can be attributed to differences in the ocean inflow, water column properties, and seabed characteristics among the seas around South Korea. There were no statistically significant differences between the radioactive concentrations of seawater and seabed samples collected before and after the Fukushima accident, and no areas with unusually high radiation levels were detected. Using the distribution coefficient (Kds) and the concentration ratio (CR) calculated from the 2011-to-2020 data, we evaluated the radiological impact on fish. The ERICA tool was utilized to assess these data, and indicated a negligible radiological risk from radioactivity in the seawater, seabed sediments, and marine biota in the South Korean Ocean.

Assessment of radiological impact on the surrounding environment and biota for phosphogypsum waste stockyard in Korean facility.

In this study, the effects of deposited gypsum residues on the surrounding environment and radiation exposure in plants and animals were evaluated under various exposure situations. A waste stockyard in a Korean facility (surrounded by mountains and sea) was used to store phosphogypsum, a byproduct of phosphoric acid processes, in a slurry form in a large gypsum storage facility (provided separately on the facility site). The ERICA tool was used to evaluate the impact of radiation on nonhuman environments for mineral processing and waste storage for risk estimation. The impact of radiation on the environment due to the phosphogypsum stockyard was negligible with a screening dose of less than 10 µGy h-1. However, to conservatively evaluate the environmental impact of rain and wind in the phosphogypsum stockyard, the soil at the interface of the stockyard, where plants could not grow, was considered as an input value, and the estimated dose rate of shrubs was found to be 45 µGy h-1. The effects of the phosphogypsum stockyard on the surrounding environment accounted for 95-100% of the total dose for internal exposure in biota. In general, radium was found to be the highest contributor to biota, and the next lead and polonium were contributors to the dose. The findings contribute to an understanding of the radiological impact of waste stored and disposed of at the facility on the environment and biota (all routes of exposure) and to developing sustainable operations and pollution monitoring policies.

Accurate measurement of uranium and thorium in naturally occurring radioactive materials to overcome complex matrix interference.

A standard addition (SA) calibration method for determining uranium and thorium in naturally-occurring radioactive materials (NORMs) was studied. Pretreatment method using fusion was established and optimized. The SA method was validated (LOD, LOQ, linearity, selectivity, and accuracy) using certified reference materials (SRM 2709a, RM-ZR, and RM-BX). The results were evaluated for bias, and a correction equation that included a contribution to the expanded uncertainty was used. All performance criteria were satisfied; the results agreed well with certified and reference values.

Electronic wastes: A near inexhaustible and an unimaginably wealthy resource for water splitting electrocatalysts.

E-wastes comprise complex combinations of potentially toxic elements that cause detrimental effects of the environmental contamination; besides their posing threat, most of the products also contain valuable and recoverable materials (Li, Au, Ag, W, Se, Te, etc.), which make them distinct from other forms of industrial wastes. Most of these value-added elements which are primarily employed in electronic goods are disposed of by incineration and land-filling. This is a serious issue besides just environmental pollution, as IUPAC recognized that such ignorance of or poor attention to e-waste recycling has put several elements in the periodic table to the list of endangered elements. Recycling these wastes utilized for electrocatalytic water splitting to produce H2. These recovered e-wastes materials are used as electrocatalysts for the water-splitting, additives to enhance reaction kinetics, and substrate electrodes as well. Recycling and recovery of value-added materials in the view of applying them to electrocatalytic water splitting with endangered elements' perspective have not been covered by any recent review so far. Hence, this review is dedicated to discussing the opportunities available with recycling e-wastes, types of value-added materials that can be recovered for water splitting, strategies exploited, and prospects are discussed in details.

Molybdenum Sulphoselenophosphide Spheroids as an Effective Catalyst for Hydrogen Evolution Reaction.

Electrocatalytic splitting of water is the most convincing and straight forward path to extract hydrogen, but the efficiency of this process relies heavily on the catalyst employed. Here, molybdenum sulphoselenophosphide (MoS45.1 Se11.7 P6.1 ) spheroids are reported as an active catalyst for the hydrogen evolution reaction (HER) and this is the first attempt to study on ternary anion based molybdenum chalcogenides. As-prepared MoSx Sey Pz catalyst reveals a unique morphology of microspheroids capped by stretched-out nanoflakes that exhibits excellent electrocatalytic activity (   j-10 mA cm-2 @ 93 mV, Tafel slope of 50.1 mV dec-1 , TOF-0.40 s-1 ) fairly closer to the performance of platinum (Pt) and predominant to those of the pre-existing Mo-chalcogenides and phosphides. Such an increase in performance stems from the copious amount of active edge sites, the presence of nanoflakes, and high circumferential area exposed by the spheroids. Besides, the electrode with MoS45.1 Se11.7 P6.1 displays excellent stability in acidic medium over 10 h of continuous operation. This work paves way for improving the catalytic activity of existing Mo-chalcogenide compounds by doping suitable mixed anions and also reveals the integral role of anions as well as their synergetic effects on the surface physiochemical properties and the HER catalysis.

Ultrahigh PEMFC performance of a thin-film, dual-electrode assembly with tailored electrode morphology.

A dual-electrode membrane electrode assembly (MEA) for proton exchange membrane fuel cells with enhanced polarization under zero relative humidity (RH) is fabricated by introducing a phase-separated morphology in an agglomerated catalyst layer of Pt/C (platinum on carbon black) and Nafion. In the catalyst layer, a sufficient level of phase separation is achieved by dispersing the Pt catalyst and the Nafion dispersion in a mixed-solvent system (propane-1,2,3-triol/1-methyl-2-pyrrolidinone).The high polymer chain mobility results in improved water uptake and regular pore-size distribution with small pore diameters. The electrochemical performance of the dual-film electrode assembly with different levels of phase separation is compared to conventional electrode assemblies. As a result, good performance at 0 % RH is obtained because self-humidification is dramatically improved by attaching this dense and phase-separated catalytic overlayer onto the conventional catalyst layer. A MEA prepared using the thin-film, dual-layered electrode exhibits 39-fold increased RH stability and 28-fold improved start-up recovery time during the on-off operation relative to the conventional device. We demonstrate the successful operation of the dual-layered electrode comprised of discriminatively phase-separated agglomerates with an ultrahigh zero RH fuel-cell performance reaching over 95 % performance of a fully humidified MEA.

Production of hydrogen and volatile fatty acid by Enterobacter sp. T4384 using organic waste materials.

In a study of hydrogen-producing bacteria, strain T4384 was isolated from rice field samples in the Republic of Korea. The isolate was identified as Enterobacter sp. T4384 by phylogenetic analysis of 16S rRNA and rpoB gene sequences. Enterobacter sp. T4384 grew at a temperature range of 10-45 degrees C and at an initial pH range of 4.5-9.5. Strain T4384 produced hydrogen at 0-6% NaCl by using glucose, fructose, and mannose. In serum bottle cultures using a complete medium, Enterobacter sp. T4384 produced 1,098 ml/l H2, 4.0 g/l ethanol, and 1.0 g/l acetic acid. In a pH-regulated jar fermenter culture with the biogas removed, 2,202 ml/l H2, 6.2 g/l ethanol, and 1.0 g/l acetic acid were produced, and the lag-phase time was 4.8 h. Strain T4384 metabolized the hydrolysate of organic waste for the production of hydrogen and volatile fatty acid. The strain T4384 produced 947 ml/l H2, 3.2 g/l ethanol, and 0.2 g/l acetic acid from 6% (w/v) food waste hydrolysate; 738 ml/l H2, 4.2 g/l ethanol, and 0.8 g/l acetic acid from Miscanthus sinensis hydrolysate; and 805 ml/l H2, 5.0 g/l ethanol, and 0.7 g/l acetic acid from Sorghum bicolor hydrolysate.

Theoretical investigation of Ti-adsorbed graphene for hydrogen storage using the ab-initio method.

Based on first-principles plane wave calculations, it was shown that boron substituted graphene with Ti metal atom adsorption can be used as a high capacity hydrogen storage material. Boron substitution in graphene enhances the Ti metal adsorption energy, which is much larger than that in the case of pure graphene, and than the Ti cohesive energy. The Ti metal atom can be well dispersed on boron-substituted graphene and can form a 2 x 2 pattern because the clustering of the Ti atoms is hindered by the repulsive Coulomb interaction between them. The H2 adsorption behavior on Ti metal atoms was investigated, along with the H2 bonding characteristics and the open-metal states of Ti. It was found that one Ti adatom dispersed on the double sides of graphene can absorb up to eight H2 molecules, corresponding to a 7.9% hydrogen storage capacity. In addition, the adsorption behaviors of non-H2 atoms like C and B were calculated to determine if Ti atoms can remain in an open-metal state in boron-substituted graphene.

Development of a four-zone carousel process packed with metal ion-imprinted polymer for continuous separation of copper ions from manganese ions, cobalt ions, and the constituent metal ions of the buffer solution used as eluent.

A three-zone carousel process, in which Cu(II)-imprinted polymer (Cu-MIP) and a buffer solution were employed as adsorbent and eluent respectively, has been developed previously for continuous separation of Cu²âº (product) from Mn²âº and Co²âº (impurities). Although this process was reported to be successful in the aforementioned separation task, the way of using a buffer solution as eluent made it inevitable that the product stream included the buffer-related metal ions (i.e., the constituent metal ions of the buffer solution) as well as copper ions. For a more perfect recovery of copper ions, it would be necessary to improve the previous carousel process such that it can remove the buffer-related metal ions from copper ions while maintaining the previous function of separating copper ions from the other 2 impure heavy-metal ions. This improvement was made in this study by proposing a four-zone carousel process based on the following strategy: (1) the addition of one more zone for performing the two-step re-equilibration tasks and (2) the use of water as the eluent of the washing step in the separation zone. The operating conditions of such a proposed process were determined on the basis of the data from a series of single-column experiments. Under the determined operating conditions, 3 runs of carousel experiments were carried out. The results of these experiments revealed that the feed-loading time was a key parameter affecting the performance of the proposed process. Consequently, the continuous separation of copper ions from both the impure heavy-metal ions and the buffer-related metal ions could be achieved with a purity of 91.9% and a yield of 92.8% by using the proposed carousel process based on a properly chosen feed-loading time.

Continuous separation of copper ions from a mixture of heavy metal ions using a three-zone carousel process packed with metal ion-imprinted polymer.

In this study, a three-zone carousel process based on a proper molecular imprinted polymer (MIP) resin was developed for continuous separation of Cu(2+) from Mn(2+) and Co(2+). For this task, the Cu (II)-imprinted polymer (Cu-MIP) resin was synthesized first and used to pack the chromatographic columns of a three-zone carousel process. Prior to the experiment of the carousel process based on the Cu-MIP resin (MIP-carousel process), a series of single-column experiments were performed to estimate the intrinsic parameters of the three heavy metal ions and to find out the appropriate conditions of regeneration and re-equilibration. The results from these single-column experiments and the additional computer simulations were then used for determination of the operating parameters of the MIP-carousel process under consideration. Based on the determined operating parameters, the MIP-carousel experiments were carried out. It was confirmed from the experimental results that the proposed MIP-carousel process was markedly effective in separating Cu(2+) from Mn(2+) and Co(2+) in a continuous mode with high purity and a relatively small loss. Thus, the MIP-carousel process developed in this study deserves sufficient attention in materials processing industries or metal-related industries, where the selective separation of heavy metal ions with the same charge has been a major concern.

Preparation and antibacterial effects of Ag-SiO2 thin films by sol-gel method.

In the present study, silver-doped silica thin films were successfully prepared by sol-gel method to apply for antibacterial materials. The starting solution was prepared from 1:0.24:3.75:2.2 molar ratios of Si(OC2H5)4):AgNO3:H2O:C2H5OCH2CH2OH and then the pH value controlled at 3 with 0.5 N HNO3 solution. The formation of silver-doped glassy silica thin films at various temperatures was investigated through infrared spectroscopy, ultraviolet-visible, scanning electron microscopy and X-ray diffraction. From these analysis data, it was found that silver ions were completely trapped in the silica matrix and their reduction could be achieved at 600 degrees C annealing temperature. The antibacterial effects of silica thin films against Escherichia coli and Staphylococcus aureus were examined by film attachment method. The coating films had an excellent antibacterial performance.

Preparation of Eu-Doped Y(2)O(3) Luminescent Nanoparticles in Nonionic Reverse Microemulsions.

In this study, Y(2)O(3):Eu luminescent nanoparticles were prepared by precipitation of aqueous yttrium nitrate/europium nitrate solution using ammonium hydroxide in the reverse microemulsions based on polyoxyethylene (5) nonylphenyl ether/polyoxyethylene (9) nonylphenyl ether, cyclohexane, and water. With Eu-doped Y(2)O(3) nanoparticles obtained, particle size, shape, chemical composition, crystalline formation rate, crystallinity, and photoluminescence were measured and compared with those of particles formed by a bulk precipitation method. The nanoparticles synthesized in microemulsion showed a narrow size distribution, spherical shape, fast crystalline formation rate, high crystallinity, and strong photoluminescence. This stronger photoluminescence of particles formed in a microemulsion might be attributed to more densely packed particles with very few voids and higher crystallinity at a relatively low temperature than those synthesized through a bulk precipitation method. Copyright 2000 Academic Press.