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| 1 | Pulse radiolysis studies of functionally substituted imidazolium-based ionic liquids显示文摘The reactions of imidazolium-based ionic liquids having different substituent groups on the ring with hydrated electrons (eaq-),hydroxyl radicals (·OH),and sulfate anion radicals (SO4·-) were investigated using nanosecond pulse radiolysis techniques.The spectra of these ionic liquids on reaction with eaq-all exhibited a similar peak at about 320 nm,and a typical peak for eaq-in aqueous ionic liquid solutions.The reaction rate constants for 1,3-disubstituted imidazolium-based ionic liquid hexafluorophosphates (BMIPF 6) with eaq-were deduced to be 10 10 L mol-1s-1,however the values were lower for trisubstituted ionic liquids.For example,the rate constant for 1-butyl-2,3-dimethylimidazolium tetrafluoroborate (BMMIBF 4) was 5.5×10 9 L mol-1s-1.Imidazolium-based ionic liquids reacted with hydroxyl radicals via adducts to produce a mixture of isomeric OH adducts,and the pk a value of the OH adducts was deduced to be 8.4±0.4 for 1-butyl-3-methylimdazolium tetrafluoroborate (BMIBF 4).Moreover,imidazolium cations were also oxidized by SO4·-to produce bivalent cation radicals,which exhibit a peak at 320 nm,and these rate constants are of the same order of magnitude,i.e.,10 9 L mol-1s-1,except that for 1-(2-hydroxyethyl)-3-methylimdazolium tetrafluoroborate with SO4·-(k=2.8×10 8 L mol-1 s-1).Theoretical calculations were carried out to estimate the structures of the products of reduction by eaq- and the results were related to the experimental data. | FU HaiYing XING ZhaoGuo CAO XiYan WU GuoZhong | 2012 | Chinese Science Bulletin2012，57，21： | 3 |
| 2 | Activation of the receptor for advanced glycation end products (RAGE) exacerbates experimental autoimmune myasthenia gravis symptoms显示文摘 | Lili Mu Yao Zhang Bo Sun Jinghua Wang Xiaoli Xie Na Li Jia Zhang Qingfei Kong Yumei Liu Zhijuan Han Guangyou Wang Zheng Fu Bo Yu Guozhong Li Hulun Li | 2011 | Clinical Immunology2011，，1： | 1 |
| 3 | Temperature-dependent structural changes of[Bmim]FeCl4 magnetic ionic liquid characterized by an in-situ X-ray absorption fine structure显示文摘The temperature-dependent structural changes in 1-butyl-3-methylimidazolium tetrafluoride([Bmim]FeCl4)magnetic ionic liquid(MIL)were investigated by using in-situ X-ray absorption fine structure(XAFS)combined with Raman spectroscopy and DFT calculations.XAFS re sults revealed that the coordination number and bond length of Fe-Cl in the anion of[Bmim]FeCl4 MIL decreased with increments in temperature.These results directly reflected the dissociation of tetrahedral structure[FeCl4]^-,and the formation of bridge-chain[Fe2 Cl5]^+,and[FeCl2]^+species in the anion of[Bmim]FeCl4 MIL.These behaviors indicated that[FeCl4]^-dissociation was endothermic,and was promoted by increased temperature.The results obtained through XAFS were in agreement with those obtained through Raman spectroscopy and DFT calculations. | Fangling Jiang Hao Peng Cheng Li Haiying Fu Guozhong Wu | 2020 | Chinese Chemical Letters2020，31，3： | 1 |
| 4 | Wear Characteristics of the Nuclear Control Rod Drive Mechanism(CRDM)Movable Latch Serviced in High Temperature Water显示文摘The current research of nuclear control rod drive mechanism(CRDM)movable latch only makes a simple measurement of wear mass.The wear volume and difference in various claw surfaces are ignored and the degradation mechanism of each claw surface is not clear.In this paper,a detailed degradation analysis was carried out on each claw surface of movable latch combined with wear result and worn morphology.Results indicate that the boundary of carbide is preferred for corrosion because carbide presents a nobler Volta potential compared to the metal matrix or boundary region.Due to the oscillation of drive shaft between the claw surfaces of movable latch,the dominant wear mechanism on the upper surface of claw(USC)and lower surface of claw(LSC)is plastic deformation caused by impact wear.Mechanical impact wear will cause the fragmentation of carbides because of the high hardness and low ductility of carbides.Corrosion promotes the broken carbides to fall off from the metal matrix.The generated fine carbides(abrasive particles)cause extra abrasive wear on USC when the movable brings the drive shaft upward or downward.As a result,USC has a higher wear volume than LSC.This research proposes a method to evaluate the wear on the whole movable latches using a 3D full-size scanner. | Tianda Yu Guozhong Fu Yanqing Yu Liting Zhu Maofu Liu Wei Li Qiang Deng Zhenbing Cai | 2022 | Chinese Journal of Mechanical Engineering2022，35，2： | 1 |
| 5 | Structural analysis of [Bmim]_2CuCl_4 ionic liquids in the presence of water and ethanol by XAFS technique显示文摘The structure of [Bmim]2Cu Cl4 ionic liquids(Bmim: 1-butyl-3-methylimidazolium) with different ratios of H2 O and C2H5 OH was investigated using X-ray absorption fine structure(XAFS) technique. In this study, XAFS was employed to directly probe the conformational variations of copper ions in [Bmim]2Cu Cl4 with the addition of either water or ethanol. XAFS analysis confirmed that the structure of ionic liquids gradually transformed from tetrahedral to octahedral configuration with the increase in ratio of H2 O. Our results also showed that water molecules coordinated with the copper ions of [Bmim]2Cu Cl4, leading to the conformational change in ionic liquids. However, the XAFS spectra of [Bmim]2Cu Cl4/C2H5 OH indicated no coordination of anhydrous ethanol with the copper ions of [Bmim]2Cu Cl4. The structure of [Bmim]2Cu Cl4 ionic liquids is maintained as the tetrahedral configuration in presence of ethanol. Therefore, anhydrous ethanol causes little variation in the structure of ionic liquids and it is a good solvent for the dilution of ionic liquids. | Fangling Jiang Cheng Li Haiying Fu Yaxing Wang Xiaojing Guo Guozhong Wu | 2015 | Science China Chemistry2015，58，4： | 0 |
| 6 | Influence of FeCl_3 on radiation stability of ionic liquid BmimCl显示文摘This study investigates the effect FeCl3 on the radiation stability of the ionic liquid,1-butyl-3-methylimidazolium chloride(BmimCl) over a wide dose range of 0 to 1000 kGy under γ-ray radiation.The ionic liquid species,BmimFeCl4,was formed by adding FeCl3 into BmimCl.The results showed that the presence of FeCl4-significantly improved the radiation resistance of BmimCl,wherein the effect was more pronounced at higher FeCl4-content.Meanwhile,under irradiation,Fe(II) was generated from Fe(III),which was reduced by solvated electron.In addition,the concentration of Fe(II) increased with low level of absorbed dose,but leveled off at higher doses.Moreover,the radiation yield of the solvated electrons of BmimCl was further estimated at approximately 0.358±0.01 μmol/J in BmimCl-7 mol% FeCl3 system. | HUANG Lei HUANG Wei FU HaiYing WU GuoZhong GUO ZhiJun WU WangSuo CHEN ShiMou | 2013 | Chinese Science Bulletin2013，58，10： | 0 |
| 7 | Property variation of ionic liquid [Bmim][AuCl_4] immobilized on carboxylated polystyrene submicrospheres with a small surface area显示文摘In order to understand the effect of surface chemical groups on the immobilized species, Au-containing imidazolium-based ionic liquid (IL) [Bmim][AuCl4] was intentionally immobilized on polystyrene (PS) submicrospheres (d~300 nm) with a very small surface area (4-10 m2/g), which possess carboxyl-moiety (COONa or COOH) on the surface. The behavior of immobilized [Bmim][AuCl4 ] on the two types of submicrospheres was investigated by transmission electron microscopy (TEM), differential scanning calorimetry (DSC), and powder X-ray diffraction (XRD). It was revealed that the melting points (Tm) of [Bmim][AuCl4 ] that had been immobilized on PS-COONa and PS-COOH submicrospheres were decreased by 2.7 and 4.1℃, respectively. The interaction mechanism between the IL and submicrosphere surface moieties was further analyzed by X-ray absorption fine structure (XAFS) analysis. The data indicated that the coordination environment of Au species changed markedly when [Bmim] [AuCl4] was immobilized on the surfaces of PS-COONa and PS-COOH submicrospheres, as illustrated by the decrease in white line peak intensity. The effect of surface COOH groups on Tm depression and the white line peak intensity of the XANES spectrum is more pronounced than that of COONa groups, most likely due to the possible hydrogen bond formation between the COOH group and [Bmim]+. | HE YaXing FU HaiYing LI Cheng JI Xiang GE XueWu ZOU Yang JIANG Zheng XU HongJie WU GuoZhong | 2013 | Chinese Science Bulletin2013，58，24： | 0 |
| 8 | Electron transfer in N-butylpyridinium tetrafluoroborate ionic liquid by pulse radiolysis显示文摘The radiolysis behavior of neat pyridinium ionic liquids (ILs) and their aqueous solutions was investigated using nanosecond pulse radiolysis techniques. Radiolysis of the ionic liquids, such as N-butylpyridinium tetrafluoroborate (BuPyBF4 ), resulted in the formation of solvated electrons and organic radicals. Solvated electrons reacted with the pyridinium moiety to produce a pyridinyl radical, which can transfer electrons to various acceptors. The electron-transfer rate constants of the solvent-derived butylpyridinyl radicals in BuPyBF 4 and in several compounds (for example, duroquinone, 4,4′-pyridine, benzophenone, and 1,1′- dimethyl-4,4′-bypyridinium dichloride) (k of the order 10 8 L/(mol s) were lower than those measured in water and in i-PrOH but were significantly higher than the diffusion-controlled rate constants estimated based on viscosity. The electron-transfer rate constants in neat BuPyBF 4 were one order of magnitude faster than the diffusion-controlled values. This finding suggests that Bu- PyBF 4 acts not only as solvent but also as active solute, such as in solvent-mediated reactions. These reactions result in electrons reaching their final destinations via intervening pyridinium groups without requiring the diffusion of a specific radical. | FU HaiYing XING ZhaoGuo CAO XiYan WU GuoZhong | 2013 | Chinese Science Bulletin2013，58，16： | 0 |
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