共查询到20条相似文献,搜索用时 62 毫秒
1.
2.
催化动力学光度法测定微量邻菲罗啉 总被引:2,自引:0,他引:2
催化动力学分析法,在国内外均有广泛的研究,并有综合性报道,但大多数是用以测定痕量无机离子,对于测定微量有机物的报道尚属少见。尤其是用催化动力学光度法测定邻菲罗啉的报道更为少见。邻菲罗啉是一种目前广泛应用的氧化还原指示剂和有机显色剂,因此研究微量邻菲罗啉测定方法具有重要意义。本文研究在0.2mol·L~(-1)的硫酸介质中,微量邻菲罗啉对过氧化氢氧化酸性络蓝K的褪色指示反应有明显地催化作用,吸光度的变化值在一定的条件下与催化剂浓度呈线性关系,借此建立了测定微量邻菲罗啉的动力学光度新催化体系。 相似文献
3.
4.
钴(Ⅱ),镍(Ⅱ)—邻菲罗啉极谱催化前波的机理研究 总被引:3,自引:1,他引:3
本文研究了Co(Ⅱ)、Ni(Ⅱ)与邻菲罗啉的极谱催化前波的反应机理。用多种实验技术,并与Eu(Ⅱ)-邻菲罗啉催化前波的活化桥机理相对比,提出了此两催化前波是电活性络合物的反应机理,也指出了两者之间的不同点。 相似文献
5.
6.
在pH 9.5的氨水-氯化铵缓冲溶液中,锰(Ⅱ)与邻菲罗啉反应生成组成比为1:1稳定且电活性的锰(Ⅱ)-邻菲罗啉络合物.采用线性扫描极谱法和循环伏安法研究了锰(Ⅱ)-邻菲罗啉络合物的电化学行为,提出了茶叶中锰含量的测定方法.对测定条件,包括支持电解质、缓冲溶液的浓度、反应介质的酸度、以及增敏剂的选择等,作了试验并予以优化,并探讨了锰(Ⅱ)-邻菲罗啉络合物极谱峰的电化学性质及电极反应机理.在优化的条件下,还原峰峰电流与锰(Ⅱ)浓度在6.3×10-8~8.0 ×10-7mol·L-1范围内呈线性关系,检出限(3S/N)为2.0×10-8mol·L-1.此法用于茶叶样品分析,加标回收率在97.8%~102.1%之间. 相似文献
7.
配合物的稳定性与配体酸碱强度之间的直线自由能关系 Ⅺ.铜(Ⅱ)-5-取代邻菲罗啉-α-氨基酸三元体系 总被引:2,自引:1,他引:2
在25.0±0.1C和0.1mol·dm-3KNO3存在下,用pH法测定了邻菲罗啉、5-硝基邻菲罗啉、5-氯邻菲罗啉、5-甲基邻菲罗啉为第一配体;脯氨酸、α-氨基异丁酸、异亮氨酸、缬氨酸、甘氨酸、丝氨酸为第二配体与铜(Ⅱ)形成三元配合物的稳定常数,结果表明三元配合物的稳定性与第一配体和第二配体的酸碱强度之间均存在直线自由能关系,应用反馈π键存在的程度讨论了配合物稳定性的变化趋势。 相似文献
8.
9.
含有不同结构第二配体的铕(Ⅲ)三元有机配合物的合成与发光 总被引:6,自引:0,他引:6
合成了3种新的1, 10-菲罗啉的衍生物: 二吡啶[3, 2-f: 2', 3'-h]喹喔啉(DPQN), 咪唑并[5,6-f]邻菲罗啉(IP)和苯基咪唑并[5,6-f]邻菲罗啉(PIP), 以它们作为第二配体, 并以二苯甲酰甲烷(DBM)为第一配体, 合成了3种新的铕(Ⅲ)三元有机配合物.通过元素分析、红外光谱、1H-核磁共振光谱确定了它们的组成, 研究了3种配合物的热稳定性、成膜性能和光致发光性能(发光强度, 荧光量子效率和寿命),并初步从理论上探讨了含有不同结构的第二配体对铕(Ⅲ)配合物发光的影响, 为筛选有机电致发光新材料提供了认识基础. 相似文献
10.
应用温度跃迁装置和断流分光光度计分别研究了铜(II)-2,9-二甲基邻菲罗啉与α-氨基酸和N-苯基乙二胺在25℃、0.1mol·dm^-^3KNO3水溶液中的生成反应动力学。实验结果表明在铜(II)-2,9-二甲基邻菲罗啉-α-氨基酸三元配合物的生成速率常数与配体α-氨基酸的酸离解常数之间存在着如下的直线自由能关系: logkf=2.84+0.53pK2。根据Eigen机理讨论了铜(II)-2,9-二甲基邻菲罗啉-N-苯基乙二胺三元配合物的生成反应动力学。 相似文献
11.
Solvent extraction studies have been made on some metals: In/III/-Tl/III/ and Hg/II/-Cd/II/-Co/II/, from ammonium thiocyanate solutions by dialkyl sulphoxides. Separation of these metals from one another can be achieved by suitable choice of the extracted conditions. The nature of the extractable metal species has been elucidated. 相似文献
12.
Summary Single reverse water-gas shift (RWGS) and dehydrogenation of propane with CO2(DH-CO2) reactions in the presence and absence of the CrOx/SiO2 catalyst have been studied between 673 and 873 K. It was found that the CrOx/SiO2 catalyst is active both in the dehydrogenation of propane and in the RWGS reactions. The obtained results suggest that the
dehydrogenation of propane to propene in the presence of CO2on CrOx/SiO2can be facilitated by the RWGS reaction.</o:p> 相似文献
13.
Synthesis of chlorobis/β-diketonato/oxotechnetium/V/ and tris/β-diketonato/technetium/III/ complexes
K. Hashimoto Y. Yamada T. Omori K. Yoshihara 《Journal of Radioanalytical and Nuclear Chemistry》1989,135(3):187-197
Chlorobis/-diketonato/ oxotechnetium/V/ complexes [TcOCl/-dik/2, -diketone=acetylacetone, benzoylacetone and dibenzoylmethane] were newly synthesized using macroamount of99Tc. These complexes were further separated into geometrical isomers. Furthermore, an improvement of the yields for the syntheses of tris/-dike-tonato/technetium/III/ complexes [Tc/-dik/3, -diketone=acetylacetone, benzoylacetone and 2-thenoyltrifluoroacetone] was examined using Tc/III/-thiourea complexes as a starting material. 相似文献
14.
Summary CexTi1-xO2 and H3PW12O40/CexTi1-xO2 catalysts were prepared using a sol-gel method, and applied to the direct synthesis of dimethyl carbonate from methanol and
carbon dioxide. H3PW12O40/CexTi1-xO2 showed a better catalytic performance than the corresponding CexTi1-xO2, due to the bifunctional catalysis of Br?nsted acid sites (provided by H3PW12O40) and base sites (provided by CexTi1-xO2). H3PW12O40/Ce0.1Ti0.9O2 showed the highest catalytic performance among the H3PW12O40/CexTi1-xO2 catalysts. 相似文献
15.
The crystal structure of trisodium monophosphate hemihydrate was determined. The space group is and a unit cell contains eight formula units. The unit cell dimensions of are a = 9.631(3), b = 5.416(2), c = 16.938(8) Å, β = 102.60(5)°. The final R value is 0.027 for a set of 1430 independent reflections. This atomic arrangement is mainly a three-dimensional network of distorted NaO6 octahedra. The hydrogen bonding scheme is given. 相似文献
16.
A series of single-phase LixNi0.8-yCo0.2ZnyOp(0.96 ≤x≤ 1.10, 0 ≤y≤ 0.05, 2 ≤p≤ 2(1+y) ) (different in the y values) were synthesized by a two-step solid state reaction method, in which LiOH·H2O, Zn-doped spherical Ni(OH)2 and Co2O3 were used as the precursors. The ICP-AES analyses proved that the Zn-doped compounds synthesized had the nonstoichiometric form. The results of the XRD, SEM identified that the uniform particles of the as-prepared materials having a good layered structure were fine, narrowly distributed and well crystallized. The electrochemical performance test was carried out and the results showed that the as-prepared Zn-doped materials had not only a high capacity, but also a better cycling stability characterization than the un-doped one. The Li1.06Ni0.75Co0.22Zn0.03O2.03 material has an initial reversible capacity as high as 160.5mAh·g-1; and a first discharge efficiency 89.2%, and exhibits satisfactory cyclic stability with 90% retainable capacity after 50 cycles. 相似文献
17.
Grisel Corro Odilón Vázquez-Cuchillo Fortino Ba?uelos 《Reaction Kinetics and Catalysis Letters》2005,87(1):171-175
Summary A strong promoting effect of the presence of C3H8or C3H6was determined for the combustion of CH4in excess oxygen, over pre-sulfated 1%Pt/g-Al2O3and pre-sulfated 1%Pt-2%Sn/g-Al2O3catalysts.</o:p> 相似文献
18.
Mónica Martos Beatriz Julián Eloisa Cordoncillo 《Journal of solid state chemistry》2007,180(2):679-687
Doped-rutile has been traditionally used in ceramic pigments for its intense optical properties. In this paper, we compare the classical ceramic synthesis of Ti1−2xNbxNixO2−x/2 system with the sol-gel methodology, which allows a reduction of the anatase-rutile transformation temperature. The composition was optimised in order to obtain a unique rutile phase with the minimum amount of pollutant Ni(II) and enhanced chromatic coordinates. Incorporation of the doping ions in the rutile structure was corroborated by XRD and Rietveld refinements. The species responsible for the colour mechanism were studied by different techniques. UV-VIS spectroscopy showed the characteristic features of Ni2+ ions, whose existence was corroborated by EPR and magnetic measurements. From these results, (Ni,Nb)doped-TiO2 powder samples can be now shaped as thin films, monoliths, etc. by using sol-gel methodology without modifying their properties. This study introduces new possibilities of coloured TiO2-based solid solutions in new combined advanced applications (colouring agent and photocatalyst, etc.). 相似文献
19.
Nitrogen substituted yellow colored anatase TiO2−xNx and Fe-N co-doped Ti1−yFeyO2−xNx have been easily synthesized by novel hydrazine method. White anatase TiO2−δ and N/Fe-N-doped samples are semiconducting and the presence of ESR signals at g ∼1.994-2.0025 supports the oxygen vacancy and g∼4.3 indicates Fe3+ in the lattice. TiO2−xNx has higher conductivity than TiO2−x and Fe/Fe-N-doped anatase and the UV absorption edge of white TiO2−x extends in the visible region in N, Fe and Fe-N co-doped TiO2, which show, respectively, two band gaps at ∼3.25/2.63, ∼3.31/2.44 and 2.8/2.44 eV. An activation energy of ∼1.8 eV is observed in Arrhenius log resistivity vs. 1/T plots for all samples. All TiO2 and Fe-doped TiO2 show low 2-propanol photodegradation activity but have significant NO photodestruction capability, both in UV and visible regions, while standard Degussa P-25 is incapable in destroying NO in the visible region The mid-gap levels that these N and Fe-N-doped TiO2 consist may cause this discrepancy in their photocatalytic activities. 相似文献
20.
采用高温固相法制备了4种高纯度晶相组成的LixZryOz三元化合物,研究了焙烧温度、时间、反应物的种类和初始反应物物质的量比对产物组成的影响,进一步用XRD、SEM及BET分析方法对产物的晶相结构、表面形貌及比表面积进行了表征.实验结果表明,Li2CO3与ZrO2在适当条件下可以合成得到单斜相Li3ZrO3;以LiOH替代Li2CO3,在适当条件下可以分别合成得到四方相Li2ZrO3和三斜/单斜相Li6Zr2O7;进一步以Zr(NO3)4·5H2O代替Zr02,可将单斜相Li6Zr2O7的制备时间由96 h缩短至24 h.SEM照片显示产物硬团聚明显,粒径分布在1~10μm间,BET分析表明样品比表面积处于1.0~9.0 m2·g-1间分布,反应过程中锂的过量以及长时间高温焙烧是引起产物粒径长大和产生硬团聚的主要原因. 相似文献