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41.
非有机溶剂萃取催化光度法测定锰Mn(Ⅱ)-H2O2-EBT-PEG-2000体系 总被引:3,自引:0,他引:3
研究了碱性介质中,利用锰(Ⅱ)催化过氧化氢氧化铬黑T的指示反应。用聚乙二醇-2000非有机溶剂萃取平衡控制反应时间和指示反应进行的程度。通过测量酸性条件下539nm处聚乙二醇-2000相的吸光度,建立了非有机溶剂萃取催化光度法测定痕量锰(Ⅱ)的新方法。方法的线性范围为0.0080~0.55μg.mL-1,检测限为3.0×10-9g.L-1,可用于铝合金、茶叶样品中锰的测定。 相似文献
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The initial stage of electrodeposition of manganese dioxide has been studied on the platinum disk electrode and on the ring-disk electrode. Two current maxima were observed on the anodic voltammograms. It has been shown that the first rise in the current is associated with the formation of manganese dioxide (MD) nuclei on the electrode surface, and the second with their growth at the border between MnO2 and bare platinum due to an increase in the perimeter of the nuclei. Electrodeposition on bare platinum proceeds at a higher rate than on the surface of growing MD. This is explained by the difference in the reaction mechanisms on these substrates. The first stage of the process on the growing MD is the chemisorption of Mn(II) ions with the formation of Mn(III) ions, which are then electrochemically oxidized to MD. Chemisorption is the slowest step in the whole process. 相似文献
45.
Minghuey Shieh Horng-Sun Chen Huey-Yea Yang Chuen-Her Ueng 《Angewandte Chemie (International ed. in English)》1999,38(9):1252-1254
The first Te–Mn–CO clusters were obtained by the thermal reaction of K2TeO3 with [Mn2(CO)10] in MeOH. The basicity of the μ4-Te ligand in the octahedral cluster anion [(μ4-Te)2Mn4(CO)12]2− is demonstrated by its binding to the fragment [(TeMe2)Mn(CO)4]+ in an axial fashion to afford the novel cluster 1 . 相似文献
46.
Zhongze Ma 《Tetrahedron letters》2008,49(11):1782-1785
To unambiguously confirm the actual product in autoxidation of salvinorin A under basic conditions, deacetyl-1,10-didehydrosalvinorin G was synthesized from salvinorin C via intermediate salvinorin H. Furthermore, oxidation of salvinorin D with manganese dioxide gave salvinorin G in good yield. 相似文献
47.
Solvothermal reaction of [MnCl2(terpy)] with elemental As and Se at a 1:1:2 molar ratio in H2O/trien (10:1) at 150 °C affords the linear trimanganese(II) complex [{Mn(terpy)}3(μ‐AsSe4)2] ( 1 ). The tridentate [AsSe2(Se2)]3? anions of 1 chelate the terminal {Mn(terpy)}2+ fragments and bridge these through their remaining Se atom to the central {Mn(terpy)}2+ moiety. Weak interactions of Mn1···Se and Mn3···Se bonds with length 2.914(7) and 3.000(7) Å link the molecules of 1 into infinite chains. Treatment of [MnCl2(cyclam)]Cl with As and Se at a 1:1:2 molar ratio in superheated H2O/CH3OH (1:1) at 150 °C yields the dinuclear complex [{Mn(cyclam)}2 (μ‐As2Se6)] ( 2 ), whose novel [(AsSe2)2(μ‐Se2)]4? ligands bridge the MnII atoms in a μ‐1κ2Se1, Se2: 2κ2Se5,Se6 manner. 相似文献
48.
This paper reports the syntheses and characterization of two phosphonate compounds with layered structures, namely, Mn2(2-C5H4NPO3)2(H2O) (1) and Zn(6-Me-2-C5H4NPO3) (2). In compound 1, double chains are found in which the {Mn2O2} dimers are linked by both aqua and O-P-O bridges. These double chains are connected through corner-sharing of {MnO5N} octahedra and {CPO3} tetrahedra, forming an inorganic layer. The pyridyl groups fill the inter-layer spaces. In compound 2, each {ZnO3N} tetrahedron is vertex-shared with three {CPO3} tetrahedra and vice versa, hence forming an inorganic honeycomb layer. The pyridyl groups reside between the layers. Magnetic studies show that weak antiferromagnetic interactions are mediated between the manganese ions in compound 1. Crystal data for 1: monoclinic, space group C2/c, , , , β=107.3(1)°. For 2: orthorhombic, space group Pbca, , , . 相似文献
49.
Investigations of the catalytic properties of manganese oxides for the oxygen reduction reaction in alkaline media 总被引:2,自引:0,他引:2
Fabio H.B. Lima Marcelo L. Calegaro Edson A. Ticianelli 《Journal of Electroanalytical Chemistry》2006,590(2):152-160
The oxygen reduction reaction (ORR) was studied in KOH electrolyte on different manganese oxides, dispersed on a carbon powder (MnOx/C). The oxides were prepared by different methods, for producing MnO, Mn3O4 and MnO2 as major phases dispersed on the Vulcan XC-72 carbon. The oxides were characterized by XRD (X-ray diffraction) and in situ XANES (X-ray absorption near edge structure). The electrochemical measurements were made using cyclic voltammetry and steady state polarization curves carried out in an ultra-thin layer rotating ring/disk electrode. The results have shown lower activity for the ORR on the MnOx/C species compared to that on Pt/C, but higher activity compared to that of pure Vulcan carbon. Formation of involving 2e− per O2 molecule is the main path of the ORR in the studied MnOx/C catalysts but, at low overpotentials and rotation rates the number of electrons is raised to 4 due to the occurrence of a disproportionation reaction. Large differences of electrocatalytic activity were seen for the different oxide species, and these were related to the presence of a Mn(IV) phase and the occurrence of a mediation processes involving the reduction of Mn(IV) to Mn(III), followed by the electron transfer of Mn(III) to oxygen. 相似文献
50.
以ZrO(NO3)2·2H2O为前驱体对多壁碳纳米管(MWCNTs)进行了改性并负载MnOx制备了MnOx/ZrO2/MWCNTs 催化剂. 考察了Zr 对催化剂低温选择性催化还原(SCR)反应活性的影响,并通过多种分析手段对催化剂的结构进行了表征. 结果表明Zr 的添加对催化剂的低温SCR活性具有显著的促进作用,当Zr 负载量为30%时,催化剂活性最佳. X射线衍射(XRD)、拉曼(Raman)光谱、透射电镜(TEM)、N2吸附-脱附的表征结果分析表明,适量的Zr 改性促进了MnOx在载体表面的分散,增强金属氧化物与MWCNTs 之间的作用,也能增加催化剂的比表面积、孔容和孔径. X 射线光电子能谱(XPS)、H2程序升温还原(H2-TPR)和NH3程序升温脱附(NH3-TPD)的分析结果则显示,Zr 能提高催化剂表面化学吸附氧浓度,促进Mn3+转化为Mn4+,从而使催化剂表面的活性位点增多,氧化还原能力增强,同时还提高了催化剂表面酸性位点的数量和强度,促进了NH3的吸附,是MnOx/ZrO2/MWCNTs 催化剂低温SCR活性提高的主要原因. 相似文献