可见光波段水分子离子吸收光谱的测量

通过光外差－磁旋转－速度调制光谱技术实现了对 Ｈ２Ｏ＋在 １６６８０～１７３００ ｃｍ－１的可见光区吸收光谱的高分辨测量，获得了Ａ２Ａ１－Ｘ２Ｂ１ 电子跃迁的（０，９，０）←（０，０，０）支带的 ７４条谱线，同时也验证了该技术高灵敏度和高信噪比的特点．

A universal thermodynamic model of calculating mass action concentrations for structural units or ion couples in aqueous solutions and its applications in binary and ternary aqueous solutions

A universal thermodynamic model of calculating mass action concentrations for structural units or ion couples in ternary and binary strong electrolyte aqueous solution was developed based on the ion and molecule coexistence theory and verified in four kinds of binary aqueous solutions and two kinds of ternary aqueous solutions. The calculated mass action concentrations of structural units or ion couples in four binary aqueous solutions and two ternary solutions at 298.15 K have good agreement with the reported activity data from literatures after shifting the standard state and concentration unit. Therefore, the calculated mass action concentrations of structural units or ion couples from the developed universal thermodynamic model for ternary and binary aqueous solutions can be applied to predict reaction ability of components in ternary and binary strong electrolyte aqueous solutions. It is also proved that the assumptions applied in the developed thermodynamic model are correct and reasonable, i.e., strong electrolyte aqueous solution is composed of cations and anions as simple ions, H2O as simple molecule and other hydrous salt compounds as complex molecules. The calculated mass action concentrations of structural units or ion couples in ternary and binary strong electrolyte aqueous solutions strictly follow the mass action law.

Orientation and Structure of Ionic Liquid Cation at Air/[bmim][BF4] Aqueous Solution Interface

The watermiscible room temperature ionic liquid 1butyl3methylimidazolium tetrafluorob orate （[bmim] [BF4]） is a model system for studying the interactions between ionic liquid and water molecules. In this work the orientational structure of the low concentrated aqueous solution of [bmim] [BF4] at the air/liquid interface was investigated by sum frequency gener ation vibrational spectroscopy. It has been found that at very low concentrations, the butyl chain exhibited a significant gauche defect, indicating a disordered conformation; and the cation ring oriented with a fairly small tilting angle at the surface. When the concentration increased, the cation ring tended to lie flat at the surface, and the gauche defects of the butyl chain decreased due to the intermolecular chainchain interactions and the consequent more ordered interfacial molecular arrangement. Additionally, the antisymmetric stretching mode in the PPP and SPS spectra exhibited a peak shift, showing that there exists more than one kind of orientation or chemical environment for the butyl CH3 group. These results may shed new light on understanding the surface behavior of watermiscible ionic liquids as well as the imidazolium based surfactants.

Probing Molecular Interactions in 1-Butyl-3-methylimidazolium Chloride-Water and 2,6-Dimethoxyphenol Mixtures Using Attenuated Total Reflection Infrared Spectroscopy

Molecular interactions of the ternary mixtures of 1-butyl-3-methylimidazolium chloride （[C4C1im]Cl）-water-2,6-dimethoxyphenol （2,6-DMP, a phenolic monomer lignin model compound） were investigated in comparison with the [C4C1im]Cl-water binary systems through attenuated total reflection infrared spectroscopy. Results indicated that the microstructures of water and [C4C1im]Cl changed with varying mole fraction of [C4C1im]Cl （xIL） from 0.01 to 1.0. This change was mainly attributed to the interactions of [C4C1im]Cl-water and the self-aggregation of [C4C1im]Cl through hydrogen bonding. The band shifts of C-H on imidazolium ring and the functional groups in 2,6-DMP indicated that the occurrence of intermolecular interactions by different mechanisms （i.e., hydrogen bonding or π-π stacking） resulted in 2,6-DMP dissolution. In the case of xIL=0.12, the slightly hydrogen-bonded water was fully destroyed and [C4C1im]Cl existed in the form of hydrated ion pairs. Interestingly, the maximum 2,6-DMP solubility （238.5 g/100 g） was achieved in this case. The interactions and microstructures of [C4C1im]Cl-water mixtures influenced the dissolution behavior of 2,6-DMP.

Organotemplate-free Hydrothermal Synthesis of SUZ-4 Zeolite: Influence of Synthesis Conditions

Various conditions were investigated in detail for the novel organic template-free static hydrothermal synthesis of SUZ-4 zeolite in the presence of seeds. The obtained samples were characterized by XRD （X-ray diffraction）, SEM （scanning electron microscope）, TG （thermal gravimetric analysis）, ICP （inductively coupling plasma） elemental analysis, nitrogen sorption isotherm and surface area. The results show that pure SUZ-4 zeolites with high crystallinity are obtained in a broad window of synthesis conditions： seed mass concentration 0.2%-2%, SIO2/A1203 molar ratio 21 25, KOH/SiO2 molar ratio 0.33 0.43, H20/SiO2 molar ratio 7.14-38.1, aging time 24 h, crystallization temperature 160℃, and crystallization time 6-10 d. Also, crystallinity and size of the rod-like SUZ-4 zeolite crystals are found to alter with the conditions.

Clay mineral expansion of black cotton soil based on interlayer cation hydration

To analyze the water swelling characteristics of black cotton soil(BCS),X-ray fluorescence and X-ray diffraction characterizations were performed to investigate the chemical compositions and types of clay minerals in BCS.A montmorillonite crystal lattice was established to simulate the hydration of interlayer cations by applying the SPC/E potential energy model,universal force field,algorithm of charge balance,and periodic boundary.Results indicated that the main clay mineral found in the BCS was montmorillonite(32.6%)with small amounts of interstratified illite-montmorillonite(10.9%),illite(2.3%),and kaolinite(1.5%).The high expansive potential of BCS comes from the strong adsorption property of montmorillonite with a high content of magnesium and sodium ions to water molecules.The exchangeable cations of Na^(+)in BCS were only 3.73%,but they enhanced the adsorption capacity of clay to water molecules and accelerated the hydration of Mg^(2+)(47.1%)and Ca^(2+)(4.78%).The free swell index can be used as a classification index of the swelling potential of BCS.

Adsorption of Cu（ll）, Ni（ll） and Pb（ll） Ions in Aqueous Solutions by a Biopolymer Chitosan at Different Molecular Weights

In this study, the feasibility of using chitosan, a multifunctional environmentally friendly biopolymer, at different molecular weights to simultaneously adsorb various metal ions from aqueous solutions was evaluated. The experiments were carried out to estimate adsorptivity and selectivity of three molecular weights chitosan, 3.60 × 105 （Chl）, 5.97 × 105 （Ch2） and 9.47 × 105 （Ch3） g/mol, towards Cu（II）, Ni（II）, and Pb（II） ions in aqueous solutions. Experimental results indicated that chitosan of high molecular weight （Ch3） was the best at adsorption capacity than the others. On chitosan solutions followed by Ni（II） and then Cu（II）. the other hand, Pb（lI） had the highest adsorption ability in the three

Antioxidative and hepatoprotective activities of the ethyl acetate fraction separated from the fruit of Livistona chinensis

OBJECTIVE:To examine the antioxidative and hepatoprotective activities of the effective fraction separated from the fruit of Livistona chinensis(FLC)and to explore the possible mechanism.METHODS:The antioxidative activities of the various fractions separated from FLC were analyzed by in vitro DPPH(1,1-diphenyl-2-picrylhydrazyl radical 2,2-diphenyl-1-(2,4,6-trinitrophenyl) hydrazyl,DPPH) radical and superoxide anion free radical(O^(2-)) scavenging assays.The potential hepatoprotective effects of the ethyl acetate fraction separated from FLC(EFLC) were examined in LO_2 cells and mice.LO_2 cells were incubated with EFLC and exposed to H_2O_2-induced oxidative stress.BABL/C mice were orally administered EFLC for consecutive7 d,and fulminant hepatitis was induced by cauda vein injection of Con A on day 7.RESULTS:EFLC showed prominent antioxidative effects in DPPH-and O^(2-) scavenging assays.EFLC pretreatment effectively protected LO_2 cells from H_2O_2-induced oxidative stress by decreasing apoptosis and raising the levels of antioxidant enzymes.Additionally,EFLC protected mice against Con A-induced fulminant hepatitis by markedly reducing the serum levels of alanine transaminase and aspartate aminotransferase,attenuating histological damage of the mouse liver,and elevating the levels of glutathione peroxidase and total superoxide dismutase,while decreasing the contents of methane dicarboxylic aldehyde,tumor necrosis factor-α,and interleukin-1β in the mouse liver.Furthermore,EFLC pretreatment downregulated the protein expression of B-cell lymphoma 2(Bcl-2) associated X protein,caspase-3,caspase-8,Fas,and Fas L,while upregulating the protein expression of Bcl-2 in the mouse liver.CONCLUSION:These findings revealed that EFLC effectively protected against in vivo and in vitro liver injury,and the mechanism is closely associated with its antioxidative and anti-apoptotic properties.