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181.
重铬酸钾氧化偶氮胂Ⅲ褪色催化光度法测定痕量钴的研究 总被引:3,自引:2,他引:3
在醋酸-醋酸钠缓冲介质中痕量钴(Ⅱ)对重铬酸钾氧化偶氮胂Ⅲ褪色反应有显著的催化作用,催化反应的表现活化能为25.62kJ.mol^-1,据此建立了测定痕量钴的催化动力学分析法,线性范围为0~350ng.mL^-1,检出限为2.0ng.mL^-1(Co),除Fe(Ⅱ)外,其余常见共存离子基本不影响钴的测定,本法重现性较好,用于测定人发,茶叶,土壤和废水中钴的含量,结果满意。 相似文献
182.
Zhuxing Tang Yun Zhou Yikun Zeng Shuliang Zang Pingang He Yuzhi Fang 《Chromatographia》2006,63(11-12):617-622
A method based on capillary electrophoresis with electrochemical detection has been developed for the separation and determination of epicatechin, isovanillic acid, vanillic acid and myricetin in Dioscorea bulbifera L. and its medicinal preparations. The effects of working electrode potential, pH and concentration of running buffer, separation voltage and injection time were investigated. Under optimum conditions, the analytes could be separated in a 40 mmol L?1 borate buffer (pH 8.7) within 15 min. A 300 μm diameter carbon disk electrode has a good response at + 0.95 V (vs. SCE) for all analytes. The response was linear over three orders of magnitude with detection limits (S/N = 3) ranging from 3.0 × 10?8 g mL?1 to 1.0 × 10?7 g mL?1. The method has been successfully applied to the analysis of real samples. 相似文献
183.
用质谱技术对钾、钙同位素体系特征参数测定的初探 总被引:1,自引:0,他引:1
报道了用FinniganMAT 2 62质谱技术和同位素稀释法测定了光谱纯CaO和国际二级标准Tahiti(CaCO3)的同位素40 Ca 42 Ca比值以及后者的40 Ca含量 ,RSD分别为 0 .0 2 %和 0 .1 %。对国家钾标样的测定表明 :39K、40 K和41 K同位素丰度分别为 0 .93 2 60± 0 .0 0 1 2、0 0 0 0 1 1 2 0± 0 .0 0 0 0 1 2 9和 0 .0 672 86± 0 .0 0 0 1 2 5。其中39K含量为 0 .1 2 1 72± 0 .0 0 0 2 9,与标准值在误差范围内一致。实验测定结果为在我国开展40 K 40 Ca同位素体系的定年和环境的示踪研究打下了基础 相似文献
184.
Wen-Jia Zhou Shu-Juan Bao Yan-Yu Liang Ben-Lin He Hu-Lin Li 《Journal of Solid State Electrochemistry》2006,10(5):277-282
Pure-phase and well-crystallized spinel LiMn2O4 powders were successfully synthesized by a simple rheological phase method. The thermal behavior and structure properties
of the powders prepared by the rheological phase method compared with the solid-state reaction were investigated by thermogravimetry,
powder X-ray diffraction , scanning electron microscopy and transmission electron microscopy. According to the results of
the electrochemical tests, it is obvious that the sample resulting from the rheological phase method shows higher discharge
capacity and better cycling stability than one formed in the solid-state reaction. The cyclic voltammogram and columbic efficiency
curves also confirm that the product by the rheological phase method has a good cycling performance due to its fine cubic
spinel structure and morphology. 相似文献
185.
Lingping Wang Aiguo Kong Bo Chen Hanming Ding Yongkui Shan Mingyuan He 《Journal of molecular catalysis. A, Chemical》2005,230(1-2):143-150
Transition metal copper substituted mesoporous silica (Cu-SBA-15) was synthesized using triblock copolymers surfactant as template agent under acidic condition. The result Cu-SBA-15 was characterized with XRD, ICP-AES, FT-IR and N2 adsorption–desorption measurements, which prove that Cu(II) was mainly incorporated into the framework of Cu-SBA-15. Its catalytic activity was studied for phenol hydroxylation using H2O2 (30%). The substituting element (Cu2+) is incorporated into the framework position forming a new type of active site which raises the phenol conversion to 62.4% and the diphenol (the mixture of catechol (CAT) and hydroquinone (HQ)) selectivity to 97%. The Cu-SBA-15 has very high selectivity for catechol (about 71% selectivity), which is completely different from that of the microporous titanium silicalite zeolites (47.1% phenol conversion and about 50% selectivity to CAT under same reaction conditions). The results obtained indicate that the selective oxidation of phenol with H2O2 by a radical substitution mechanism. 相似文献
186.
Ce0.6Zr0.35Y0.05O2和Pr0.6Zr0.35Y0.05O2催化剂表面上CO氧化和18O-16O交换反应的研究 总被引:5,自引:0,他引:5
测定了在Ce0.6Zr0.4O2,Ce0.6Zr0.35Y0.05O2,Pr0.6Zr0.4O2和Pr0.6Zr0.35Y0.05O2 (分别表示为CZ,CYZ,PZ和PYZ)样品表面上的CO氧化反应和18O-16O 同位素交换反应.结果表明: 在CZ和PZ系列固熔中掺杂Y3 离子可以改善晶格氧的迁移速度;PZ和PZY的晶格氧比CZ 和CZY 的晶格氧具有更高的氧化反应活性.其原因是将Y3 掺杂到Ce0.6Zr0.4O2 或Pr0.6Zr0.4O2晶格中,增加了样品的氧空位浓度,从而提高了晶格氧的迁移性质,而PrOx比CeO2具有更低温度的氧化还原性质,因此PZ和PZY的晶格氧比CZ 和CZY 的晶格氧具有更高的氧化反应活性. 相似文献
187.
188.
手性配体的空间结构与产物对映选择性的关系 总被引:2,自引:0,他引:2
首次采用4-烷氧羰基噻唑烷、E唑烷作为手性配体,诱导烷基锌对醛类的亲核加成反应,获得产物是烷基化的醛,最高达90%ee,产率98%的(S)-二级醇。系统地考察了该类手性配体三维空间结构变化与产物对映选择性的关系,当配体4-位烷氧羰基上的R、2-位R′基和环体上原子X发生变化时都会引起产物(S)-二 级醇的对映选择性发生规律性变化。对五种不同结构的底物醛在同一手性配体催化下,诱导烷基锌对醛类的亲核加成反应,底物结构变化也会引起(S)-二级醇对映选择性变化。 相似文献
189.
Besides the running buffer, pH of buffer, separation voltage and sampling time, the diluting agent was studied in this paper as one of the important factors influencing the sensitivity in capillary electrophoresis (CE) with amperometric detection (AD) when electrokinectic sampling was used. Clonidine hydrochloride, hydrochlorothiazide and rutin, which are positively charged, neutral and negatively charged, respectively, in aqueous solutions, could be perfectly separated by CE with 25 mmol x L(-1) Na(2)B(4)O(7) - 50 mmol x L(-1) NaH(2)PO(4) as running buffer and detected by measuring their current responses with AD. Before CE running, some kinds of diluents including water, methanol, formamide, running buffer, hydrochloric acid and sodium hydroxide were, respectively, applied to dilute the stock solutions of above three analytes and their effects on the sensitivity of CE-AD were investigated. The results showed that for electrokinetic injection, the current responses of these three analytes were greatly affected in different ways when different diluting agents were used. This method was applied to simultaneously determine the active ingredients in one Chinese compound hypotensor named Zhen Ju Jiang Ya Pian, in which the contents of clonidine hydrochloride, hydrochlorothiazide and rutin is very different as 0.03 mg : 5 mg : 20 mg per tablet, and satisfactory results were obtained by adjusting their sensitivity by selecting the suitable diluting agent. 相似文献
190.
Fe-Co-Ni合金纳米线有序阵列的模板合成与磁性 总被引:10,自引:0,他引:10
以二次阳极氧化的氧化铝膜为模板,用电化学沉积的方法成功地合成了Fe-Co-Ni三组份有序纳米线阵列.扫描电子显微镜(SEM)和透射电子显微镜(TEM)观察表明纳米线表面光滑、有序、高长径比;磁性测量表明,其矫顽力较同组份的膜材料有较大的提高.将样品在惰性气体氛围中不同温度下退火,随着退火温度增加,其纵向矫顽力有一个极值,而对应的横向矫顽力没有类似的变化,关于这一现象的机理,本文进行了初步的讨论. 图5参15 相似文献