The ambiguity of complex regional pain syndrome (CRPS) posed a challenge to many medical researchers in the early days after its discovery and continues to do so till date. The establishment of the Budapest Criteria of the International Association for the Study of Pain resolved certain queries on CRPS. Many aspects of CRPS, such as pathophysiology and etiology, remain unknown. Therefore, of these aspects, we focused on the genetic basis of CRPS. In this qualitative review, we summarized the recent findings on the genetic association of CRPS and analyzed the roles of genes identified in each study and limitations of the studies. In particular, we confirmed the reliability of each study by comparing the following research, which used the following control groups or the same candidate genes. Notably, specific phenotypes of CRPS with dystonia indicate a significant association with human leukocyte antigen (HLA)-DQ8. Further, HLA-DQ8, which is associated with aberrant CD4+ T-cell reaction, could be associated with CRPS etiology since an increased CD4+ T-cell population was reported in CRPS patients. In addition, matrix metalloproteinase (MMP)-9 found in genome-wide expression profiling is noteworthy since MMP-9 is associated with neuro-inflammatory reactions. Despite these suggestions on the genetic aspects of CRPS, the pathophysiology and etiology of CRPS may be polygenic and multifactorial, influenced by multiple genes and other factors. Further, some studies have suggested that CRPS phenotypes have different etiologies. Thus, further studies with the precise classification of CRPS on a unified basis and with a significant number of case groups are required

This paper explores the L2 motivation of 11 students about to start studying English as junior college English majors. The participants took part in a ten-day L2 motivational program designed to help them with L2 skills and life on campus. To understand how they participated in the program, data gathered from online learning logs were coded using qualitative thematic analysis. Consequently, the participants shifted to embody ‘none to something’ qualities in terms of L2 selves and effort during the program. That is, they established self-images to believe in when using and learning English, which eventually developed into effort-driven attitudes and behavior. The students also set goals and plans according to their L2 selves created or revealed during the program. Although the program was comparatively short with a small number of participants entering a junior college, the findings indicate that an L2 motivational program for new adult students could be conducive to promoting and sustaining their effort, L2 selves, and motivation.

본 연구에서 Tetraneura triangula 를 국내에서 처음으로 보고한다. 이 종의 분포지역, 기주식물, 형태학적 정보를 제공하였다.

본 연구에서 Kaltenbachiella japonica를 국내에서 처음으로 보고한다. 이 종의 분포지역, 기주식물, 형태학적 정보를 제공하였다.

The aim and originality of our current study are to use the original biomass (activated carbon) obtained by functionalizing waste banana peels (commonly found in Turkey) with acid in NaBH4 methanolysis and to examine its contribution to the hydrogen generation rate (HGR). Our study consisted of three stages. In the first stage, the optimum conditions were determined by examining the catalyst under parameters such as different acid types, different carbonization temperatures, and different carbonization times. Thus, based on the maximum HGR value, the optimum conditions were determined as H3PO4, 600 °C, and 40 min. In the second step, the effects of parameters such as acid concentration, NaBH4 concentration, catalyst amount, and temperature on HGR were investigated. As a result of methanolysis experiments (condition: catalyst amount: 100 mg, acid amount: 30%, NaBH4 concentration: 2.5%, temperature: 30 °C, carbonization temperature: 400 °C, and carbonization time: 40 min.), the maximum HGR value, the reaction completion time and activation energy were found as 65,625 mLmin− 1gcat−1, 0.233 min, and 4.56 kJ/mol, respectively. It was observed that the obtained activation energy was lower than that of some catalysts available in the literature. In addition, the structural and morphological examination of the banana peel (catalyst) with high HGR and low activation energy revealed that the acid functionalization process was successfully carried out.

In this work, we report a direct preparation of a few-walled carbon nanotube (FWCNTs) and NiMgAl composites namely FWCNT-NiMgAl by pyrolysis of waste high-density polyethylene (HDPE) plastic at 800 °C with NiMgAl-layered double hydroxide (LDH) as catalysts. The composite formation is carried out in a single step using our lab-developed pyrolysis reactor. The NiMgAl-LDH catalyst was prepared by co-precipitation method and the FWCNTs were grown on the NiMgAl-LDH catalyst with FWCNT yield of 10% and FWCNT-NiMgAl composite yield of 55% whose quality is determined by Raman ID/IG ratio of 2.57. The average outer and inner diameter of the FWCNT are found to be 5.5 nm and 2.9 nm, respectively, from TEM and 2.92 nm from the outer RBM (radial breathing mode) band, which indicates the formation of a few-walled CNTs. FWCNT-NiMgAl is used for the fabrication of flexible supercapacitor electrodes on a polyethylene terephthalate (PET) sheet which achieved a specific capacitance of 432 Fg− 1 in a wide potential range (ΔV = 2) at a scan rate of 5 mV s− 1 in 2 M KOH electrolyte with a high energy density of 240 Wh kg− 1, whereas NiMgAl displayed a capacitance of 200 Fg− 1 with an energy density of 111 Wh kg− 1. The diffusion-type charge storage mechanism (pseudocapacitance) is found to be dominant with contributions of 73.2% and 69.75% for NiMgAl and FWCNT-NiMgAl, respectively. The highest specific capacitance and energy density are obtained for NiMgAl in 2 M KCl and for FWCNT-NiMgAl in 2 M NaOH electrolytes. However, the largest potential window is observed in KOH electrolyte for both NiMgAl and FWCNT-NiMgAl with value of ΔV = 2 V. The electrode material shows good stability in acidic electrolytes and also shows good capacitive stability at high frequencies maintaining a phase angle of 70°. The present work is a novel approach to fabricate low-cost multifunctional carbon composite nanomaterials and will contribute to the research on low-cost waste-derived CNT composite preparation and its application in flexible energy storage devices.

There is an ever growing interest in the development of biochar from a large variety of agrowastes. Herein, the main objective is the conversion of pomegranate peel powder biochar and its post-functionalization by phosphoric acid treatment, followed by arylation organic reaction. The latter was conducted using in situ-generated diazonium salts of 4-aminobenzoic acid ( H2N-C6H4-COOH), sulfanilic acid ( H2N-C6H4-SO3H) and Azure A dye. The effect of diazonium nature and concentration on the arylation process was monitored using thermal gravimetric analysis (TGA) and Raman spectroscopy, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). SEM pictures showed micrometer-sized biochar particles with tubular structure having about 10–20 μm-wide channels. SEM studies have shown that arylation did not affect the morphology upon arylation. The porous structure did not collapse and withstood the arylation organic reaction in acid medium did not collapse upon arylation. TGA and Raman indicated gradual changes in the arylation of biochar at initial concentrations 10– 5, 10– 4 and 10– 3 mol L− 1 of 4-aminobenzoic acid. The detailed Raman spectra peak fittings indicate that the D/G peak intensity ratio leveled off at 3.35 for 4-aminobenzoic acid initial concentration of 10– 4 mol L− 1, and no more change was observed, even at higher aryl group mass loading. This is in line with formation of oligoaryl grafts rather than the grafting of new aryl groups directly to the biochar surface. Interestingly, Azure A diazonium salt induced much lower extent of surface modification, likely due to steric hindrance. To the very best of our knowledge, this is the first report on diazonium modification of agrowaste-derived biochar and opens new avenues for arylated biochar and its applications.

To solve the problem of water pollution, researchers have proposed a photocatalytic degradation technology, in which the key factor is the development of efficient photocatalytic materials. Graphitic carbon nitride (g-C3N4), an n-type semiconductor, has been widely studied due to its suitable band gap (2.7 eV), low cost, easy preparation, non-toxicity, and high photostability. However, the pure-phase g-C3N4 still has defects such as low specific surface area, insufficient visible light absorption, low charge mobility, few active sites for interfacial reaction, and easy recombination of photogenerated electron–hole pairs, which leads to the lower photocatalytic activity of g-C3N4. Aiming at the problems mentioned above, this paper focus on the synthesis of g-C3N4-based composites with high photocatalytic activity via lemon juice induction method. Thiourea and lemon juice were selected as precursors, and carbon quantum dots (CQDs) as electron mediators were introduced anchoring on the surface of g-C3N4 to build g-C3N4/CQDs with compact interface. The results showed that small-sized CQDs are uniformly distributed on the surface of g-C3N4, and the g-C3N4/CQDs composite has a 2D0D structure, which reduces the recombination of photogenerated electron–hole pairs. The photocatalytic degradation efficiency of 4% g-C3N4/CQDs for RhB reaches the highest data of 90.9%, and the photocatalytic degradation rate is 0.016 min− 1, which is about 2.3 times that of g-C3N4. After four cycles of photocatalytic reaction, the photocatalytic degradation efficiency of the material remained at 81.7%. Therefore, the g-C3N4/CQDs synthesized via lemon juice induction has a more stable microstructure, and the charge separation efficiency is greatly improved, which is suitable for practical photocatalytic environmental protection.

Antioxidants are food additives that extend the shelf life of food products by preventing lipid rancidity caused by active oxygen. They can either be naturally-derived or manufactured synthetically via chemical synthesis. In this study, method validation of five synthetic antioxidants, namely butylated hydroxyanisole, butylated hydroxytoluene, tertiary butylhydroquinone, propyl gallate, and disodium ethylenediaminetetraacetic acid, was performed using a high performance liquid chromatography–ultraviolet visible detector, and the method applicability was evaluated by analyzing foods containing antioxidants. The coefficient of determination (R2) average was 0.9997, while the limit of detection and limit of quantification were 0.02–0.53 and 0.07–1.61 mg/kg, respectively. The intra and inter-day accuracies and precisions were 83.2±0.7%–98.7±2.1% and 0.1%–5.7% RSD, respectively. Inter-laboratory validation for accuracy and precision was conducted using the Food Analysis Performance Assessment Scheme quality control material. The results satisfied the guidelines presented by the AOAC International. In addition, the expanded uncertainty was less than 16%, as recommended by CODEX. Consequently, to enhance public health safety, the results of this study can be used as basis data for evaluating the intake of synthetic antioxidants and assessing their risks in Korea.

Molten salts based on magnesium chloride can be used in the nuclear power reactor because they have a high heat capacity and heat stability, and allow for a faster neutron spectrum. However, magnesium chloride is highly hygroscopic, leading to the formation of moisture-related impurities, which result in the corrosion of structural materials and negatively affect the operation of the reactor. The dehydration of magnesium chloride is studied using both thermal and electrochemical treatments. According to previous studies, water impurities in magnesium chloride molten salt transform into magnesium oxide over 650 degrees Celsius. The temperature profile of the molten salt is suggested to separate magnesium chloride and magnesium oxide, focusing on cooling rate near the freezing point of magnesium chloride. Two layers separated by a phase boundary on the salt surface appear due to the density difference between magnesium oxide and magnesium chloride. Further, the removal of oxide ions remaining in the molten salt is carried out by electrochemical treatment. Two different cells, each consisting of two electrodes, are used. One cell is composed of graphite anode and nickel cathode. The other is composed of tin oxide anode and nickel cathode. As the reaction proceeds, carbon dioxide and oxygen are generated in graphite and tin oxide, respectively, and magnesium electrodeposition occurs at the cathode. The amount of purified magnesium oxide is measured to the endpoint, which is notified by the reduced current. The efficiency of each method is compared by measuring the weight ratio of the purified part to the unpurified part. Thermogravimetric analyzer (TGA) and UV-vis spectroscopy are used to check the quality of the purified part. Only magnesium oxide remains at a temperature above the boiling point of magnesium chloride. Therefore, the amount of magnesium oxide in the purified part can be measured by the mass change of the salt through the TGA method. For UV-vis spectroscopy, the transmittance is measured which depends on the weight percent of the impurities in the purified part. The suggested purification method using both thermal and electrochemical treatment is assessed quantitatively and qualitatively. It is expected that hygroscopic molten salts other than magnesium chloride will be able to be dehydrated through the above process.

Molten chloride salts are promising candidates as a coolant for Molten Salt Reactors (MSRs) because of their low cost, high specific heat transfer, and thermal energy storage capacity. The NaCl- MgCl2 eutectic salts have enormous latent heat (430 kJ/kg) and financial advantage over other types of molten chloride salt. Despite the promise of the NaCl-MgCl2 eutectic salt, problems associated with structural material corrosion in the MSR system remain. The hygroscopicity of NaCl-MgCl2 and high MSRs operating temperature accelerate corrosion within structural alloys. Especially, MgCl2 reacts with H2O in the eutectic salt to produce HCl and Cl2, which are known to further exacerbate corrosion by the chlorination of structural materials. Therefore, several studies have worked to purify impurities associated with MgCl2, such as H2O. Thermal salt purification of NaCl-MgCl2 eutectic salt is one method that reduces HCl and Cl2 gas generation. However, MgO and MgOHCl are generated as the byproduct of thermal purification through a reaction between MgCl2 and H2O. The corrosion behavior of MgO within structural alloys after thermal treatment is not well known. This paper demonstrates corrosion behavior within structural alloy after thermal treatment at various temperature profiles of the NaCl-MgCl2 eutectic salt. According to the temperature range, MgCl2·H2O are separated at 100~200°C, and MgOHCl and HCl begin to occur at 240°C or higher. Finally, MgOHCl produces MgO and HCl at 500°C or higher temperatures. After thermal treatments, the H2O, MgOHCl, and MgO content were measured by Thermo Gravimetric Analyzer (TGA) to evaluate significant products causing corrosion. The structural materials were analyzed by the Scanning Electron Microscope-Energy Dispersive Spectroscopy (SEM-EDS) and using the mass change method to observe the type of localized corrosion, the corrosion rate, and the corrosion layer thickness. This study is possible in that it can reduce economic costs by reducing the essential use of expensive, high-purity molten salts because it is related to a substantial financial cost problem considering the amount of molten salt used in industrial sites.

In 2018, media reports raised issues related to radon released from building materials used as finishing materials in apartment houses. Accordingly, related ministries recommended not to use materials with a radiation index value exceeding 1. In order to calculate the radioactivity index, not only 226Ra producing radon (222Rn) but also 232Th and 40K radioactivity concentrations are required. To determine the concentration of the radionuclide, 40K is measured by a single gamma ray of 1,460.8 keV. And the 228Ac used to measure 232Th mainly utilizes gamma rays of 911.2 keV. However, 228Ac does not appear as a single peak unlike 40K, and appears as multiple peaks at various energies. Among them, gamma rays are emitted at a intensity of 0.83% at 1,459.2 keV, which is likely to interfere with 40K. Therefore, what is actually measured at 1,460.8 keV is theoretically a compound peak of 40K and 228Ac. Because the probability of emission at 1,459.2 keV (0.83%) is low, a low concentration of 232Th will result in little 40K radioactivity error. However, samples containing a high concentration of 232Th overestimate the 40K radioactive concentration, so correction is required. In this study, the IAEA standard substance (IAEA-RGTh-1) ontaining 232Th of actual high concentration was analyzed, and the results of the analysis without correction of 40K were compared and verified. As the 40K correction method, the 911.2 keV gamma-ray of 228Ac was used as the reference peak to separate the peak of 228Ac (1,459.2 keV) from the 40K (1,460.8 keV) mixed peaks. And, the coefficient value obtained by subtracting the peak of 228Ac (1,459.2 keV) from the 40K (1,460.8 keV) mixed peak was set to a pure peak of 40K and the radioactivity concentration was calculated therefrom. As a result of calculating the IAEA-RGTh-1 reference material without correction, it was confirmed that the 40K value was overestimated by about 38 times. If a measurement beyond the MDA of 40K is generated by 228Ac radioactivity because the 40K correction constant is not applied, there is an error in determining that there is 40K radioactivity. However, even if 40K radioactivity is overestimated due to the high concentration of 232Th, the degree to which this effect contributes to the radioactivity index is very small. However, as an analyst, 40K radioactivity correction should be made for more accurate analysis.