Frontiers in Materials
·
2022
·
IF 3.985
Chang Shuangshuang,Jia Yanhong,Du Xin,Guo Shaoqiang
Pyroprocessing of spent nuclear fuels uses the LiCl–KCl molten salt as an electrolyte, which contains dissolved fission products and can be very corrosive to the structural alloys. This study investigates the effect of EuCl3 on the corrosion behavior of four commercial alloys: Haynes C276, Inconel 600, Incoloy 800, and 316L stainless steel. Static immersion tests and electrochemical polarization measurements were carried out in molten LiCl–KCl salts with and without EuCl3 additives at 500°C. The results showed that the presence of EuCl3 caused the severe dissolution of Ni, Fe, and Cr from alloys, accompanied by the cathodic reduction of EuCl3 to EuCl2. All alloys suffered from intergranular dissolution and cracking, with additional pitting and void attacks for Incoloy 800 and 316L stainless steel.
研究领域:
材料科学
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核能工程
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产品关联
DOI
高影响因子
JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE
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2025
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IF 3.5
Jun-Long Mao,Jing-Jing Fu,Min Zhang,Yan-Wei Yuan,Yue-Wen Chen
BACKGROUND Partially replacing NaCl with KCl under ultrasound can improve muscle quality and reduce oxidative degeneration of myofibrillar proteins in semi-dried large yellow croaker ( Larimichthys crocea ). Myosin, the most important protein in myofibrillar protein, plays an important role in muscle quality. Hence, the present study aimed to investigate the effect of replacing NaCl with KCl on the physicochemical properties of myosin derived from large yellow croaker under ultrasound. Furthermore, the application potential of ultrasound to low sodium salt products was evaluated. RESULTS The results showed that ultrasound treatment reduced the aggregation and particle size of myosin. By contrast, at high salt concentrations, myosin oxidation was inhibited and protein aggregation increased. This led to an increase in particle size and a decrease in stability and surface hydrophobicity of myosin. Interestingly, KCl increased myosin solubility and promoted protein unfolding, the excess of which exposed some active sites, leading to oxidative destruction of the proteins. In the present study, the chromophore and surface hydrophobic groups of myosin were exposed as a result of the KCl-mediated unfolding of the α -helices of myosin after the partial replacement of NaCl with KCl. This improved the structural stability of myosin and reduced its oxidative damage. CONCLUSION The findings of the present study show that the presence of NaCl and KCl in the system was more conducive to protecting the key role of myosin in the muscle tissue compared with NaCl alone. Additionally, the study provides insights into the mechanism of K + and Na + action on myosin under ultrasound, along with a theoretical basis for the application of ultrasound in low sodium salt products. © 2025 Society of Chemical Industry.
研究领域:
食品科学
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生物化学
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产品关联
DOI
PubMed
高影响因子
PROCEEDINGS OF THE COMBUSTION INSTITUTE
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2016
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IF 4.12
Erwei Leng,Yang Wang,Xun Gong,Biao Zhang,Yang Zhang,Minghou Xu
The influence of KCl and CaCl 2 on the primary reactions of cellulose pyrolysis is studied using a wire-mesh reactor from 250 °C to 600 °C, focusing on the reaction intermediates. A pre- column derivatization with benzoyl chloride prior to HPLC analysis is applied for the quantification of anhydro-sugars (levoglucosan, cellobiosan, maltosan) from pyrolysis. At low temperatures, the additions of inorganics salts, especially CaCl 2 , weakens hydrogen bonds, resulting in high yields of levoglucosan and cellobiosan from the cleavage of glycosidic bonds rather than from dehydration reactions . At elevated temperatures, dehydration reactions in the sugar units are mainly responsible for the destruction of sugar rings followed by the scission of pyran rings, leading to the weight-loss of CaCl 2 -loaded cellulose in the form of low molecular weight organic species. Meanwhile, accumulated unsaturated structures suppress the cleavage of glycosidic bonds, leading to the formation of char. However, KCl appears to catalyze the cleavage of glycosidic bonds or the scission of pyran rings directly, which perhaps occurs through a homolytic mechanism, leading to low molecular weight species. Furthermore, maltosan is shown to be a secondary product and is catalyzed by KCl and CaCl 2 indirectly through the repolymerization of levoglucosan in the solid phase. A modified mechanism is also proposed regarding cellulose pyrolysis and the primary catalysis of KCl and CaCl 2 .
研究领域:
化学工程
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能源科学
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DOI
高影响因子
RSC Advances
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2019
·Vol. 9
·期 46
·26718-26728
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IF 3.049
Wei Han,Wenlong Li,Jiazhuang Chen,Mei Li,Zhuyao Li,Yongchang Dong,Milin Zhang
Cyclic voltammetry, square wave voltammetry, linear polarization, chronopotentiometry and chronoamperometry were performed to investigate the electrochemical properties of Y(III) on W and Pb electrodes in LiCl–KCl eutectic melts. The diffusion coefficient of Y(III) measured by various techniques was in the order of 10−5. The nucleation of Y on W electrode was found to comply with the instantaneous nucleation mechanism. With increasing temperature, the exchange current densities increased and the charge-transfer resistances decreased, and exchange current densities are distinctly larger on liquid Pb electrode compared with W electrode. In addition, the co-deposition mechanism of Y(III) and Pb(II) on W electrode was also studied and four Pb–Y intermetallics could be detected. The feasibility of extraction metallic Y from the melts was explored by co-deposition on W electrode and under-potential deposition on liquid Pb electrode and the extracted products consisted of Pb3Y and Pb phases.
研究领域:
材料科学
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电化学
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
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IF 5.518
Shuai Wang,Junfeng Feng,Hui Pan
In this work, a nitrogen-doped lignin-derived hierarchical porous carbon material (LDMCN-700–2) was synthesized by a facile and green strategy using alkali lignin as carbon source, melamine as nitrogen source, and KCl as salt template. The as-prepared LDMCN-700–2 possessed unique structural properties such as a large surface area of 1012.5 m 2 ·g −1 , high nitrogen content of 4.5 at%, and hierarchical porous structure with micropores, mesopores and macropores, which endow it with superior electrochemical performance . The electrochemical measurements demonstrated that LDMCN-700 as an electrode material exhibited a high specific capacitance of 245 F·g −1 at 0.5 A·g −1 , as well as excellent cycling stability with 95.7 % capacitance retention after 5000th cyclic voltammetry cycles, indicating its great potential for supercapacitors .
研究领域:
材料科学
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能源存储
✓ 已验证
DOI
高影响因子
JOURNAL OF CHEMICAL AND ENGINEERING DATA
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2018
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IF 2.196
Lingzong Meng,Xia Wang,Dan Li,Tianlong Deng,Yafei Guo,Lan Yang
The solubilities in the quaternary system NaCl–KCl–SrCl2–H2O and its subsystem KCl–SrCl2–H2O at 288.15 K were investigated with the isothermal dissolution method. The phase diagram of the ternary system is composed of two single-salt crystallizations for KCl and SrCl2·6H2O, two solubility univariant curves, and one cosaturated point. The dry-salt diagram of the quaternary system consists of three single-salt crystallization fields for NaCl, KCl, and SrCl2·6H2O, three solubility univariant curves, and one invariant point. By combination of the determined solubilities and Pitzer binary parameters obtained in the literature, the lacking Pitzer mixing parameters θNa,Sr, θK,Sr, ΨNa,Sr,Cl, and ΨK,Sr,Cl and the solubility product constants of the solid salts for the systems were fitted on the basis of the Pitzer model. The model was then used to calculate the solubilties of the two systems. The theoretical results calculated using the model coincide with the experimental values.
研究领域:
化学热力学
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无机化学
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产品关联
DOI
高影响因子
RUSSIAN JOURNAL OF INORGANIC CHEMISTRY
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2023
·Vol. 67
·期 1
·S78
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IF 2.1
Han H. J.,Ma J. J.,Xing K. Q.,Shao D. X.,Zhong S. K.
Abstract In this work, the equal-water activities for the ternary system LiCl−KCl−H 2 O and its sub-binary systems LiCl−H 2 O were determined using an isopiestic method at 323.15 K. The determined isopiestic composition lines for the LiCl−KCl−H 2 O system were found to deviated Zdanovskii rule high with increasing ionic strength of the mixture solution. The addition of KCl to an aqueous solution of LiCl was found to decrease and increase the water activity at low and high LiCl molality. The Pitzer–Simonson–Clegg (PSC) model was used to represent the experimental determined water activities of the titled system and the calculated values are discussed. Based on the calculated results, the turning point appears at about 17.0 mol kg −1 LiCl solution.
研究领域:
化学
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物理化学
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产品关联
DOI
高影响因子
METALLURGICAL AND MATERIALS TRANSACTIONS B-PROCESS METALLURGY AND MATERIALS PROCESSING SCIENCE
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2017
·Vol. 48
·期 5
·2535-2542
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IF 1.642
Zhang Zhong-Lin,Zhou Lin-Zong,Ji De-Bin,Yan Yong-De,Hong Wei,Liu Yu-Hui,Wang Pu,Yin Tai-Qi,Zheng Jia-Ning,Xue Yun,Ye Yuan-Feng
Electrochemical behavior of Nd was studied in NaCl-KCl melt on W and Cu electrodes via cyclic voltammetry and chronopotentiometry. Generally, the reduction of Nd 3+ takes place in two consecutive steps in molten chlorides, such as LiCl-CaCl 2 , LiCl-BaCl 2 , CaCl 2 -NaCl, LiCl-KCl melts. However, the reduction of Nd 3+ ions was found to be through a one-step process: Nd 3+ + 3e − → Nd. The co-reduction behavior of Nd 3+ and Cu 2+ ions and the mechanisms of alloy formation were investigated in NaCl-KCl melt on W electrodes at 988 K (715 °C). Four potential plateaus corresponding to four different kinds of Cu-Nd intermetallic compounds were detected. Cu-Nd alloys were prepared on Cu electrodes at 988 K (715 °C) and 1143 K (870 °C). At 988 K (715 °C), Cu 5 Nd phase was identified by X-ray diffraction. The morphology and micro-zone chemical analysis of the alloys were characterized by scanning electron microscopy equipped with energy-dispersive spectrometry. The alloy film was observed on the Cu electrodes. Moreover, at 1143 K (870 °C), a globate bulk Cu-Nd alloy with Cu 5 Nd, Cu 4 Nd, Cu 2 Nd, CuNd, and Cu phases, as liquid in the melt, was obtained at the bottom of the crucible.
研究领域:
材料科学
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电化学
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产品关联
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2015
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IF 4.504
Yanqing Cai,Hongxia Liu,Qian Xu,Qiushi Song,Liang Xu
The in-situ preparation of LiCl–KCl–ZrCl 4 melt was investigated by the replacement reaction between Zr and CuCl in LiCl–KCl melt at 500 °C, and the reaction progress was also investigated by a series of electrochemical techniques, such as cyclic voltammetry , square wave voltammetry and open circuit chronopotentiometry . The electrochemical signals show that the concentration of Zr(IV) ions increases gradually and then reaches to the maximum value with the reaction time increasing from 0 to 180 min, while the concentration of Cu(I) ions decreases rapidly and drops to below the detection limit of the electrochemical tests. Meanwhile, the concentrations of Cu and Zr ions in the melt were determined over time by chemical analysis in the course of reaction. The results are in good agreement with the electrochemical tests. Finally, LiCl–KCl melts with (0.837 wt.% ∼ 1.709 wt.%) ZrCl 4 are obtained, and the final concentration of Cu(I) in the melt has dropped to below 0.025 wt.% when the reaction lasted for 180 min.
研究领域:
材料科学
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电化学
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产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2017
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IF 3.387
Xi Zhang,Yan Xu,Yong Zhou,Yinyan Gong,Yongli Huang,Chang Q Sun
An incorporation of the hydrogen bond (O:H O or HB) cooperativity notion, contact angle detection, and the differential phonon spectrometrics (DPS) has enabled us to gain refined information on the HCl, KCl and KOH solvation resolved solute-solvent molecular interactions and the solution surface stresses. Results show that ionic polarization stiffens the solvent H O bond phonon from 3200 to 3480 cm −1 in the hydration shells. The HO − in alkaline solution, however, shares not only the same H O phonon redshift of compressed water from 3200 to < 3100 cm −1 but also the dangling bonds of H 2 O surface featured at 3610 cm −1 . Salt and alkaline solvation enhances the solution surface stress by K + and Cl − ionic polarization. The excessive H + proton in acid solution forms a H↔H anti-HB that depresses the solution surface stress, instead. The solute capability of transforming the fraction of the O:H O bonds of the solvent matrix is featured by: f H = 0 and f x ∝ 1-exp(-C/C 0 ) (x = HO − , K + and Cl − ) towards saturation. Exercises not only confirm the presence of the H↔H anti-HB point fragilization, the O:⇔:O super-HB point compression, and ionic polarization dominating the performance of the respective HCl, KOH, and KCl solutions, but also demonstrate the power of the DPS that enables high resolution of solute-solute-solvent interactions and correlation between HB relaxation and solution surface stress.
研究领域:
化学
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物理化学
✓ 已验证
DOI
高影响因子
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2024
·Vol. 171
·期 12
·122503
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IF 3.1
Yanhong Jia,Hong Zhang,Ahmet Burak Çubuk,Biao Wu,Shaoqiang Guo
A mesh-type assembly and stirrer assembly were developed to improve the performance of liquid cadmium cathodes for the electrodeposition of U and Ce from LiCl-KCl molten salt at 773 K. The thermodynamic basis for electrodepositing U and Ce was established through the calculation of equilibrium potentials and cyclic voltammograms, while also examining the co-deposition of Li. Thereafter, U and Ce electrodeposition was performed by galvanostatic electrolysis, and the current efficiency was determined. It was found that both assemblies effectively hampered the growth of U dendrites and Ce-Cd dendritic alloys. However, the utilization of the mesh-type assembly resulted in a greater current efficiency for U, with the maximum deposited amount attaining 7.7 wt% U/Cd without causing U dendrites formation. In contrast, the current efficiency for Ce was enhanced after using the stirrer assembly due to an improved diffusion flux of Ce ions. Finally, cathode deposits were characterized by scanning electron microscopy, energy-dispersive spectroscopy, and X-ray diffraction, which revealed that disrupted fine U dendrites were randomly scattered in the Cd bulk, and that the CeCd11 dendritic alloys were also damaged, leading to an increased atomic ratio of Ce to Cd at the Cd bottom.
研究领域:
材料科学
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电化学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF CHEMICAL AND ENGINEERING DATA
·
2015
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IF 2.037
Haijun Han,Dongdong Li,Lijiang Guo,Yan Yao,Haitang Yang,Dewen Zeng
Water activity for binary KCl–H2O, NaCl–H2O and MgCl2–H2O, as well as two ternary NaCl–MgCl2–H2O and KCl–MgCl2–H2O, systems has been measured by using an isopiestic method at 323.15 K. The isopiestic results obtained show that the isopiestic composition lines of the NaCl–MgCl2–H2O system was found to obey the Zdanovskii rule, whereas the KCl–MgCl2–H2O system was observed to deviate slightly. The experimental water activities determined were applied to regress the parameters of the Pitzer model with a good agreement. The model with new parameters is validated by comparing water activity predictions with those given in the literature and not used in the parametrization process and calculating the solubility of the NaCl–MgCl2–H2O and KCl–MgCl2–H2O systems at various temperatures with the comparison of literature values.
研究领域:
化学
·
热力学
✓ 已验证
DOI
高影响因子