Two new coordination polymers,[Ln（oba）（ox）0.5（H2O）2]n（Ln = Ho（1）,Eu（2）;H2oba = 4,4？-oxybis（benzoic acid）,H2ox = oxalic acid） have been synthesized under hydrothermal conditions.According to single-crystal X-ray diffraction analyses,complex 1 crystallizes in the monoclinic system,space group P21/c with a = 13.783（2）,b =10.0120（15）,c = 12.1974（18） ,β = 105.217（2）°,V = 1624.2（4） 3,C15H12O9Ho,Mr = 501.18,Z = 4,Dc = 2.050 g/cm3,F（000） = 964,μ = 4.919 mm-1,λ（MoKα） = 0.71073 ？,GOOF = 1.124,the final R = 0.0239 and wR = 0.0570 for 3310 independent reflections with Rint = 0.0298.Complexes 2 and 1 are isostructural.Oba and ox ligands bridge the Ln（III） ions into 2D layers with（4,4） topology,which are further interlinked into a 3D supramolecular network by hydrogen bonds.TG curves of the two complexes are studied to examine their thermal stabilities.Additionally,complex 2 shows red fluorescence in the solid state at room temperature.
One-dimensional strontium hydroxyapatite （Sr-HAp） nanorods were successfully synthesized by a simple solvothermal method. The products were characterized via X-ray diffraction （XRD）, Fourier transform infrared （.FT-IR）, .cold field emission.sc.anning.elec.tron microscopy_.（FESEM）, transmission.electron microscopy （TEM）,photoluminescence （PL） excitation and emission spectra. The experimental results indicated that oleic acid as a surfactant played a key role in confining the growth of the Sr-HAp powders. A possible formation mechanism of the one-dimensional nanorod was proposed and elaborated. Moreover, the as-obtained Sr-HAp samoles showed an intense and bright emission band centered at 460 nm under long-wavelength UV light excitation and the contents of NaOH used in the synthetic process had an obvious impact on the optical performance of Sr-HAp powders. The possible luminescent mechanism of the Sr-HAp samples was discussed.
采用反相悬浮聚合法,以(NH4)2S2O8-NaHSO3为引发剂,N,N’-亚甲基双丙烯酰胺(MBA)为初体交联剂,环氧氯丙烷(ECH)为表面交联剂,单体丙烯酸(AA)和丙烯酰胺(AM)与羧甲基纤维素钠(CMC)接枝共聚,制得含有阴离子亲水基团和非离子亲水基团的颗粒状高吸水性树脂,研究了表面交联剂的加入量及表面交联时间对树脂吸水性能、保水性能及使用寿命的影响。结果表明表面强化交联与单一交联的产品相比,具有更高的吸液率、吸液速率、脱水速率和使用寿命。通过表面强化交联,树脂的吸水能力可提高一倍以上。在优化的反应条件下,所得树脂在自来水中的吸水率为114 g g 1,在1%NaCl盐水中的吸水率为69 g g 1,吸收至半饱和量的时间小于15 s,吸收至饱和量只需1 min。吸水后的树脂无黏性、分散性好,具有一定的凝胶强度。
Two types of metal-loaded visible-light-driven photocatalysts,Mo-BiVO4and Ag-BiVO4,were synthesized by wet impregnation method.Material poperties were characterized by UV-vis diffuse reflectance spectroscopy,X-ray diffraction,field emission scanning electron microscopy,X-ray photoelectron spectroscopy and low temperature nitrogen adsorption-desorption.Photocatalytic activity of the obtained materials was investigated through degrading methylene blue(MB) solution under visible-light irradiation.The results reveal that both metal loaded-BiVO4catalysts have monoclinic scheelite structure.Mo and Ag exist as oxides on the surface of the particles.The changes of absorption in visible-light region,band gap(E g) and specific surface area(A BET) caused by loading Ag are more obvious than those caused by loading Mo.But the isoelectric point of Ag-BiVO4decreases less than that of Mo-BiVO4does.Both catalysts show higher photocatalytic activity than pure BiVO4,resulting in the significantly improved efficiency of degradation of MB.And the degradation efficiency of these two metal-loaded BiVO4photocatalysts is similar to each other.However,mechanisms of such enhancement are different.The decrease of isoelectric point helps Mo-BiVO4improve the degradation efficiency.As for Ag-BiVO4,the augmentation of absorption in visible-light region as well as the abatement of E g plays more important roles.
LIU KunJieCHANG ZhiDongLI WenJunCHE PingZHOU HuaLei
An alkaline precipitation method was introduced to produce hydrous cerium oxides.The prepared powder was characterized by Brunauer-Emmett-Teller（BET） nitrogen adsorption-desorption,X-ray diffraction（XRD）,Fourier transform infrared（FTIR） spectrometry,and thermal gravimetry（TG） approaches.The adsorbent has a chemical formula of CeO2·nH2O（n 2） and a cubic fluorite-type structure after high temperature treatment.Adsorption capacity of different temperature treated hydrous cerium oxides does not directly correlate with BET specific surface area.Phosphate adsorption isotherms follow the Langmuir equation below the treatment temperature of 800°C.Phosphate adsorption causes no change on the structure of a hydrous cerium oxides,and no signs of CePO4 precipitates are found.The ion-exchanging structure of hydrous cerium oxide plays a fundamental role in phosphate adsorption.The structure is highly temperature resistant and forms adsorption sites which adsorb both water and some anions.Complete loss of adsorption ability cannot be achieved unless the treatment temperature is higher than 1200°C.Mechanism study shows that the adsorption of phosphates is mainly an anion-exchange process.
