水溶性Rh-BISBIS配合物对阿维菌素催化加氢的研究

The hydrogenation of avermectin catalyzed by [RhCl(COD)]_2-BISBIS[COD:1,5-cyclooctadiene,BISBIS:sulfonated 1,1'-bis(diphenylphosphino Methyl-2,2'-biphenyl)] in situ in aquenous/organic two-phase system was studied.The influence of various parameters,such as the surfactant concentration,the molar ratio of rhodium to phosphine,the reaction temperature and pressure on this hydrogenation were investigated.The results showed that the hydrogenation activities of diphosphine was higher that of monophosphine.     

金属离子对Ru-Pt/γ-Al2O3催化剂上对氯硝基苯选择加氢反应的影响

 采用混合醇还原法制备了聚乙烯吡咯烷酮(PVP)稳定的Ru-Pt/γ-Al2O3双金属催化剂,考察了其催化对氯硝基苯(p-CNB)选择加氢反应的性能,探讨了反应温度、压力、第三金属离子的种类、添加量及添加方式对反应的影响. 结果表明,以Ru-Pt/γ-Al2O3为催化剂,在1.0 MPa和50 ℃的条件下反应1 h,p-CNB的转化率可达48.2%,生成对氯苯胺(p-CAN)的选择性为87.3%. 在反应体系中添加适量的Fe3+或Sn4+离子时,在相同的反应条件下,p-CNB的转化率和p-CAN的选择性分别提高到100%和99.0%. Fe3+或Sn4+的添加量及添加方式对p-CNB的转化率有较大的影响,加入Fe2+,Co2+和Ni2+离子也有利于提高催化剂的活性和选择性. Ru-Pt/γ-Al2O3催化剂体系对其它氯硝基苯的加氢反应也有明显的催化作用.     

模函数的H(o)lder连续性与次可乘性

研究了模函数(ψ)K(a,r)的H(o)lder连续性及次可乘性,建立了(ψ)K(a,r)的几个精确不等式.     

线上线下相融合的教学模式在大学数学教学中的应用与实践

构建了基于翻转课堂的混合式教学模式,将线上教学与线下教学相融合,来培养学生解决复杂问题的综合能力.教学形式呈现先进性和互动性,学生学习具有自主性,课程结构具有开放性,学习协作性等特点.采用线上线下混合式的教学模式,将知识、能力、素质有机融合,努力去构建课前、课中、课后一体化的教学环境.     

Effect of Different Energy Sources on Ochrobactrum anthropi Bacteria Chromium Reduction

Ochrobactrum anthropi CTS-325 isolated from a chromium-contaminated site had better resistance to Cr(Ⅵ) in LB medium under aerobic condition.Meanwhile,it was found that the reduction of Cr(Ⅵ) is not complete during the experimental process.Therefore,a series of small molecule energy sources including nitrogen and carbon sources were added into the LB medium in the bacterial stationary phase to promote the chromium reducibility.The result showed that the bacterial growth was positively correlated with the chromium reduction.SDS-PAGE analysis indicated that the protein groups were changed when the bacteria were stimulated by the chromium.Additionally,it was revealed that O.anthropi CTS-325 could utilize the cheaper alternative of sugar(sucrose residue leaching solution) well for further growth and restart the chromium reduction,which offered a new method for practical appli-cations.     

Fully differential cross sections for C6+ single ionization of helium

The three-Coulomb-wave(3C) model is applied to study the single ionization of helium by 2 MeV/amu C6+ impact.Fully differential cross sections(FDCS) are calculated in the scattering plane and the results are compared with experimental data and other theoretical predictions.It is shown that the 3C results of the recoil peak are in very good agreement with experimental observations,and variation of the position of the binary peak with increasing momentum transfer also conforms better to the experimental results.Furthermore,the contributions of different scattering amplitudes are discussed.It turns out that the cross sections are strongly influenced by the interference of these amplitudes.     

Effect of initial-state target polarization on the single ionization of helium by 1-keV electron impact

We report new results of triple differential cross sections for the single ionization of helium by 1-KeV electron impact at the ejection energy of 10 eV. Investigations have been made for both the perpendicular plane and the plane perpendicular to the momentum transfer geometries. The present calculation is based on the three-Coulomb wave function. Here we have also incorporated the effect of target polarization in the initial state. A comparison is made between the present calculation with the results of other theoretical methods and a recent experiment [Drr M, Dimopoulou C, Najjari B, Dorn A, Bartschat K, Bray I, Fursa D V, Chen Z, Madison D H and Ullrich J 2008 Phys. Rev. A 77 032717]. At an impact energy of 1 KeV, the target polarization is found to induce a substantial change of the cross section for the ionization process. We observe that the effect of target polarization plays a dominant role in deciding the shape of triple differential cross sections.     

Selective Hydrogenation of Avermectin Catalyzed by Iridium-Phosphine Complexes

A series of new iridium complexes, IrCl（COD）（TMOPP） （1） [COD=1,5-cyclooctadiene, TMOPP=tris（4- methoxyphenyl）phosphine], IrCl（COD）（TFMPP） （2） [TFMPP = tris（4-trifluoromethylphenyl）phosphine], IrCl（COD）（BDNA） （3） [BDNA= 1,8-bis（diphenylphosphinomethyl）naphthalene], IrCl（COD）（BISBI） （4） [BISBI= 2,2＇-bis（diphenylphosphinomethyl）biphenyl] and IrCl（COD）（BDPB） （5） [BDPB= 1,2-bis（diphenylphosphinomethyl）benzene], were synthesized and characterized by NMR spectra and elemental analyses. In order to obtain the relationships between complex structures and their catalytic properties, IrCl（COD）（DPPM） （6） [DPPM = bis（diphenylphosphino）methane], IrCl（COD）（DPPE） （7） [DPPE= 1,2-bis（diphenylphosphino）ethane], IrCl（COD）（DPPP） （8） [DPPP=1,3-bis（diphenylphosphino）propane] and IrCl（COD）（TPP） （9） [TPP=triphenylphosphine], were also synthesized according to the reported methods. The hydrogenation results showed that the low electronic density at the central metal was favorable to increase the catalytic activity for the hydrogenation of avermectin, but decrease the selectivity to ivermectin. The complex with a large chelating ring and a bulky chelating backbone would easily cause the cleavage of C-O bond in avermectin to give a byproduct avermectin aglycon.     

Surface Changes of Ochrobactrum Anthropi in Cr（Ⅵ） Treatment for 1 Hour

Bioremediation has been a considerable method for treating Cr（VI） contamination. Bacterial surface changes of Ochrobactrum anthropi during Cr biosorption was investigated in this study. We found that Cr adsorption capacity increased with the increase of initial Cr（Ⅵ） concentration. Atomic force microscope （AFM） morphologic analysis combined with surface roughness analysis indicated that the bacterial surfaces became rougher during Cr uptake process. X-ray photoelectron spectroscopy （XPS） showed that Cr（Ⅲ） was adsorbed on the bacterial surfaces. Fourier transform infrared （FT-IR） analysis showed that surface functional groups including C-O and C-N might be involved in the Cr biosorption process.