994 resultados para cold vapor-ICP-AES
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本研究应用微波消解ICP-AES 法对62 个小麦品种及3 个地区土壤的锌铁硒含量进行了分析测定,发现不同小麦品种中微量元素含量差异很大,姊妹系间也存在差异。含铁量最高与最低的小麦品种铁含量相差29.68mg/kg。含锌量最高与最低的小麦品种锌含量相差46.70 mg/kg。含硒量最高与最低的小麦品种硒含量相差0.056 mg/kg。对不同地点的小麦及土壤中锌铁硒含量进行方差分析,发现双流和西昌两地种植小麦的铁含量和硒含量均有显著差异,西昌和荣县种植的锌含量有显著差异。在3 个地点中双流种植小麦硒含量最高,西昌种植小麦的铁和锌含量最高。 通过对小麦微量元素含量与土壤中微量元素含量进行了相关性分析,结果表明:小麦中的锌铁含量与土壤中的锌铁含量呈显著正相关,土壤中铁与锌含量呈极显著正相关,小麦中铁与锌含量也呈极显著正相关。随着土壤微量元素锌铁的提高,小麦中的锌铁元素含量同时提高,而且小麦对两种元素的吸收互相促进。土壤中的硒含量与锌铁含量呈负相关。小麦中硒含量也与锌铁含量也呈负相关。说明锌和铁与硒互相拮抗。小麦硒含量与土壤硒含量呈正相关,但不显著。表明土壤硒含量可以影响小麦硒含量,但不是决定因素,小麦硒含量与小麦自身因素有关。 对姊妹系G290(高硒含量)和G289(低硒含量)进行抗重金属胁迫和抗旱性实验发现,高硒品种G290的抗逆性优于低硒品种G289。 利用RAPD 技术对7 个姊妹系进行遗传差异分析发现,高硒材料G290出现了特异条带,分别标为1、2、3、4,其他姊妹系品种中未发现特异条带,回收4 条特异条带并连接转化,得到目的片段1、2、3 的重组子,进行测序。NCBI 中结果显示没有找到植物中的同源序列,说明特异序列可能是未发现的基因片段,推测可能与小麦硒含量有关,有待进一步研究。 以上研究结果,对小麦营养研究及功能性小麦的筛选和栽培具有指导作用。 In this study, we determinated the contents of zinc, iron, selenium in 62 wheat cultivars and soil samples of three regions by method of microwave digestion/ ICPAES,found that there was great difference of zinc, iron, selenium contents in different wheat cultivars as well as different sister lines. Iron content difference was 29.68 mg/kg between the highest-iron-content cultivar and the lowest one, and zinc content difference was 46.70 mg/kg , selenium content difference was 0.056 mg/kg. Anova analysis was made on contents of zinc, iron, selenium in wheat and soil samples of different locations, significant differences of Fe and Se contents were found between wheat in Shuangliu and Xichang, significant difference of Zn content was found between wheat in Xichang and Rongxian. Se content in wheat of Shuangliu was highest, Fe and Zn contents in wheat of Xichang were highest. Relativity analysis was made on three trace elements in Wheat and in soil, the result showed that there was significant positive correlation of zinc, iron content between in Wheat and in soil, as well as between Fe and Zn both in wheat and in soil. With the improving of Zn, Fe contents in soil, contents of Zn and Fe in wheat increased and absorption of Zn and Fe in wheat will mutual promote. Negative correlation of Se and Zn contents was found in wheat and soil, but not significant, that meant the antagonism of Se and Zn. Positive correlation of Se content in wheat and soil was found. High selenium content G290 and low selenium content G289 in sister lines were selected for heavy metal stress and drought resistance experiments, the result showed that the resistance of high-selenium-content cultivar was better than low selenium one. Analysis on genetic difference was made by RAPD, and specific bands were selected, marked 1,2,3,4, no more specific bands were found in other sister lines.4 bands were recovered, ligated to T-vector and transformed E.coli. Three recombinant plasmids were obtained and sequenced. NCBI Blast showed there was no homology with other plants. It implied that these fragments probably be new genes and maybe were related to selenium in wheat. It needs further research. This paper would be useful for the study of wheat nutrition as well as selection and cultivation of functional wheat.
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By characterizing fresh and used Mo/HMCM-22 catalysts with ICP-AES, XRD, NH3-TPD technique, UV - Vis DRS and UV Raman spectroscopy, the reactivity of Mo species for methane partial oxidation into formaldehyde were directly studied with a new point of view. By comparing the fresh and used catalysts, it was found that the tetrahedral Mo species bonding chemically to the support surface were practically unchanged after the reaction, while the polymolybdate octahedral Mo species, which had a rather weak interaction with the MCM-22 zeolite, leached out during the reaction, especially when the Mo loading was high. Correspondingly, it was found from the time-on-stream reaction data that the HCHO yield remained unchanged, while COx decreased with the reaction time during the reaction. By combining the characterization results and the reaction data, it can be drawn that the isolated tetrahedral molybdenum oxo-species (T-d) is responsible for HCHO formation, while the octahedral polyoxomolybdate species (O-h) will lead to the total oxidation of methane.
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结合国内外的研究进展,综述了环境介质中硒的各种检测方法。其中重点介绍了比较常用的测定方法,如原子吸收光谱法(AAS)、原子荧光光谱法(AFS)和电感耦合等离子体原子发射光谱法(ICP-AES)等,并展望了硒在检测方法上的发展趋势。
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Arabinogalactan derivatives conjugated with gad olinium-diethylenetriaminepentaacetic acid (Gd-DTPA) by ethylenediamine (Gd-DTPA-CMAG-A(2)) or hexylamine (Gd-DTPA-CMAG-A(6)) have been synthesized and characterized by means of Fourier transform infrared spectra (FTIR), C-13 nuclear magnetic resonance (C-13 NMR), size exclusion chromatography (SEC), and inductively coupled plasma atomic emission spectrometry (ICP-AES).
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The nano-scale luminescent complex of Terbium(III)-trimesic acid (TMA)-1,10-phenanthroline(phen) was successfully synthesized by co-precipitation method in this paper. The chemical formula of the synthesized complex was speculated to be Tb(TMA)(phen)(0.0125)center dot 5H(2)O by elemental analysis, inductively coupled plasma-atomic emission spectroscopy (ICP-AES), and Fourier-transform infrared spectroscopy (FTIR). XRD pattern of Tb(TMA)(phen)(0.0125)center dot 5H(2)O indicated that it was a new crystalline complex since the diffraction angle, diffraction intensity and the distance of crystal plane were all different from those of the two ligands. TG curve proved that the synthesized nano-scale luminescent complex was stable in the range from ambient temperature to 464 degrees C in air. TEM images showed that the complex was spherical shape with an average size of 40 nm.
Resumo:
用真空电弧熔炼合成了稀土基AB2 型合金.真空电弧合成的稀土基AB2 型合金不具有Laves Phase 的单相结构,而是由多相组成.用XRD、SEM和XPS 对多次充/放电循环后电极合金结构、形貌进行了分析,用ICP-AES 分析电介质溶液中电极合金组成元素的含量,探索了稀土基AB2 型合金作为金属氢化物电极的衰变机理.实验结果表明:腐蚀是稀土基AB2 型合金氢化物电极合金结构变化和电化学性能衰变的主要原因.
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Macromolecular conjugates of two kinds of natural polysaccharides, that from Panax quinquefolium linn (PQPS) and Ganoderma applanatum pat (GAPS), with gadolinium-diethylenetriaminepenta-acetic acid (Gd-DTPA) have been synthesized and characterized by means of FTIR, elementary analysis and ICP-AES. Their stability was investigated by competition study with Ca2+, EDTA (ethylenediaminetetraacetic acid) and DTPA. Polysaccharide-bound complexes exhibit T-1 relaxivities of 1.5-1.7 times that of Gd-DTPA in D2O at 25degreesC and 9.4T. MR imaging of Sprague-Dawley (SD) rats showed remarkable enhancement in rat liver and kidney after i.v. injection of these two complexes: liver parenchyma 60.9+/-5.6%, 57.8+/-7.4% at 65-85 min; kidney 144.9+/-14.5%, 199.9+/-25.4% at 10-30 min for PQPS-GdDTPA, GAPS-Gd-DTPA at gadolinium dose of 0.083 and 0.082 mmol/kg, respectively. Our preliminary in vivo and in vitro study indicates that the two kinds of polysaccharide-bound complexes are potential tissue-specific contrast agents for MRI.
Resumo:
Arabinogalactan-Gd-DTPA was synthesized by the reaction of diethylenetriaminepenta-acetic acid (DTPA) bisanhydride with polysaccharide in dry DMSO and characterized by FTIR, elemental analysis and ICP-AES. Its stability was investigated by competition with Ca2+, EDTA, DTPA. The t(1)-relaxivity is 8.06 mmol(-1) . L . s(-1) in D2O, 8.48 mmol(-1) . L . s(-1) in 0.725 mmol . L-1 BSA, respectively. t(1)-weighted MR imaging of rat kidney and liver showed a remarkable enhancement post injection of Arabinogalactan-Gd-DTPA. The results indicate that the arabinogalactan-Gd-DTPA is a potential contrast agent for MRI.
Resumo:
碳电极表面的修饰在电化学和材料科学中很重要 .最近 ,通过层与层电子间的相互作用来自组装修饰玻碳电极已引起人们的关注 [1] .运用这种方法可将一些功能团修饰到电极表面 ,赋予电极一些新的功能 [2 ] .过渡金属取代的多金属氧酸盐不仅在配位环境 ,而且在催化活性方面都类似于金属卟啉和其它大环配体金属配合物 [3] .将其修饰到玻碳电极表面已有文献报道 [4 ] .由于修饰电极的厚度可控、成分可调及具有良好的电催化活性 ,在生物传感器和电子器件等方面具有潜在的应用前景 .取代型夹心型多金属氧酸盐具有大摩尔质量和高电荷密度 ,表现出优秀的磁性和催化活性 [5] ,将成为玻碳电极表面的修饰材料 .我们首次制备了四铁取代的夹心型钨砷酸盐 Na12 [Fe4 ( H2 O) 2 ( As2 W15O56 ) 2 ]·41 H2 O,通过元素分析 ,IR,UV和 NMR对其进行了表征 ,并通过自组装将其修饰到玻碳电极表面形成多层膜 .此修饰电极对 NO- 2 和 H2 O2 具有电催化活性 ,可望成为检测 NO- 2 和 H2 O2 浓度的探针 .1 实验部分1 .1 仪器和试剂 ICP- AES等离子体发射光谱仪 ...
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合成了阿拉伯半乳聚糖修饰的 DTPA钆配合物 ,用红外光谱、元素分析、 ICP-AES等手段进行了表征 ,用竞争性方法研究了其在水溶液中的稳定性 ,测试了其在水中及 BSA溶液中的弛豫性能 ,并进行了体内成像实验 .结果表明 ,其弛豫效率是目前临床所用造影剂 Gd-DTPA的 1 .5~ 2 .0倍 ,对肝脏和肾脏 MRI信号具有良好的增强效果 ,是比较好的潜在磁共振成像造影剂
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用电感耦合等离子体原子发射光谱法 (ICP AES)测定了 11种东北大豆中大量、小量和微量元素。比较了两种湿法消解方法 ,HNO3 HClO4,HNO3 H2 SO4和干灰化法对分析结果的影响。由于大豆含有较多的油脂 ,用混合酸消解时费时较长且需加入较多的酸 ,从而可能产生较高的背景空白 ,因此对大豆样品的前处理采用干灰法较为合适。大豆中钾和磷是大量元素 ,本工作还研究了钾和磷对其他元素测定的影响。结果表明 ,大豆中钾和磷对其他微量元素的测定没有影响。结果还表明 ,这 11种大豆中的各微量元素的含量没有显著性差异
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The effect of LB monolayers on the mixed crystal was investigated by using X-ray photoelectron spectroscopy (XPS), Transmission electron microscopy (TEM), and Inductively coupled plasma-atomic emission spectroscopy (ICP-AES). The results show that LB monolayer has selectivity for the different nucleation ions with equal charge numbers and about the same ion radius. The selectivity is dependent on the head groups of monolayer. The monolayer and the doped ions have also an effect on the crystal morphology. (C) 2000 Published by Elsevier Science B.V. All rights reserved.
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The charactesistics of two-dimension spectra obtained by inductively coupled plasma atomic emission spectrometry (ICP-AES) with charge injection detection (CID) in frequency domain were studied in the present paper. The measurement spectra were Fourier transformed and the frequency distribution of the spectra was obtained. Results showed that the spectra in frequency domain could he divided into two parts:high frequency and low frequency signals. The later stood for measurement spectra and the former for background and noises. However, the high frequecny signals could not be smoothed simply to reduce noises because the background was deteriorated even though the spectral signal did not change significantly.
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A method for the analysis of mussel standard reference material by inductively coupled plasma atomic emission spectrometry( ICP-AES) and inductively coupled plasma mass spectrometry(ICP-MS) was developed. K, Na, Ca, Mg, P, Al, Fe, Zn, Mn and Sr were determined by ICP-AES and As, B, Cd, Co, Cr, Cu, Ga, Ge, Mn, Mo, Ni, Pb, Se, Sr, U and V by ICP-MS, The interference coefficients at the Mn-55, Se-78, Cu-63, Co-59, Ni-58, Ni-60, As-75, Se-77, V-51, Cr-53 and Cr-52 originating from polyatomic ion of the matrix elements (KO)-K-39-O-16, K-39(2), (ArNa)-Ar-40-Na-23, (CaO)-Ca-43-O-16, (CaO)-Ca-42-O-16, (CaO)-Ca-44-O-16, (PO2)-P-31-O-16, (ArCl)-Ar-40-Cl-35, (ArCl)-Ar-40-Cl-37, (ClO)-Cl-35-O-16, (ClO)-Cl-37-O-16 and (ArC)-Ar-40-C-12 were determined under the selected operation parameters. The major matrix elements, such as K, Na and Ca, result in the suppression of analytes signals. The apparent concentration at the significant biological element which was produced by the different digestion methods, (.) HNO3 + H2O2 (3 + 2), HNO3 + HClO4 (3 + 0.5) and HNO3 + H2SO4 (3 + 0.5),was determined. The sample digested by HNO3 + H2O2 did not give rise to interfere on the analyte, and the backgrounds of Se-77, Ga-69, Zn-67, As-75, V-51, Cr-53 and Cr-52 were increased by HNO3 + HClO4 digestion method, that affected the determination of these elements, especially the monoisotope As and V. Sample digested by HNO3 + H2SO4 increased the backgrounds at Cu-65, Zn-64 and Zn-67. Detection limits of ICP-AES are 0.001 similar to 0.75 mg/L and those of ICP-MS are 0.005 similar to 1.01 mu g/L. The relative standard derivations of ICP-AES and ICP-MS are 2.7% similar to 12.8%, 3.4% similar to 24.8%, respectively.
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将目标因子分析用于电感耦合等离子体原子发射光谱分析(ICP-AES)对高纯氧化铥中稀土杂质的测定及光谱重叠干扰校正.数据矩阵由纯光谱矢量、混合物光谱矢量及模型背景矢量构成.提出利用各目标矢量的真误差的平方和为评价函数优化扫描光谱峰位,从而消除扫描式ICP光谱仪发射光谱线的峰位移动给测定带来的影响