共查询到20条相似文献,搜索用时 0 毫秒
1.
《Analytical letters》2012,45(19):2445-2452
Abstract A new spectrophotometric method for vanadium determination is proposed. The method is based on the extraction in Adogen-toluene solution of the complex formed between V(V) and o-Aminobenzohydraxámic acid The method allows determination of 50 to 110 μg of V(V). The error and the apparent molar absorptivity are 1.2% and 5.2 ± 103 l.mol?1. cm?1 respectively. The interferences caused by foreign ions have been established. The method is applied with success to determination of vanadium in petroleum crudes. 相似文献
2.
3.
《Analytical letters》2012,45(14):1733-1742
Abstract A method is described for the spectrophotometric determination of vanadium by measuring its colored complex with salicylic acid in formic acid medium. Lambert-Beer's law is followed in the range of 2.0 - 32.0 μg V/ml of the final solution. Thirty-six ions were tested and did not interfore, at the established conditions. 相似文献
4.
《Analytical letters》2012,45(11):2063-2075
Abstract A new, sensitive and selective method for separation, and extraction - spectrophotometric determination of V (V) with pyrogallol {Ar (OH)3} and hydroxyamidines (HOA) is described. The molar absorptivities of the colored species with six substituted HOA lie in the range of (0.52–1.5)x 106 L mole?1 cm?1 at λmax 430–440 nm. Of these, the simplest compound, N-hydroxy-N, N- diphenylbenz-amidine (HDPBA) gives the most sensitive color reaction and hence, it is used for detailed studies. No interference of almost all diverse ions tested is noticed. The method offers the determination of vanadium in different environmental samples. 相似文献
5.
6.
测定化探样品中痕量钒的流动注射光泽精化学发光法 总被引:4,自引:1,他引:3
用配有Jones还原器的流动注射系统,研究了光泽精与钒(Ⅱ)的化学发光反应,并建立了钒的流动注射化学发光分析法。该法线性范围为1×10-6~1×10-2 g/L ,检出限为3×10-7 g/L,相对标准偏差为2.0 %(1×10-4 g/L,n=11),相关系数在0.9988以上。已用于化探样品中痕量钒的测定,结果令人满意。 相似文献
7.
A new and simple extraction spectrophotometric method for the determination of vanadium(V) with KIO4, N‐phenylbenzohydroxamic acid (PBHA) and crystal violet (CV), in industrial waste water samples is described. It is based on the extraction of mixed‐ligand complex V(V)‐IO4? ‐PBHA‐CV+ into chloroform solution over 2‐7 MHC1. The molar absorptivity of the complex is (7.20) × 1031 mol?1 cm?1 at λmax 535 nm. The detection limit of the method is 44 μg 1?1 V. The linearity of the calibration curve is followed up to 6 μgmL?1 in the organic solution with slope, intercept and correlation coefficient of 1.34 × 10?1, 6.7 × 10?3 and +0.99, respectively. This method enhances the sensitivity of the conventional PBHA method for the determination of vanadium, and is free from interferences of other metal ions commonly associated with vanadium. The method has been successfully tested for the determination of V in the industrial waste water samples. 相似文献
8.
9.
同时测定合成样中铜钴镍钒含量的分光光度法--主成分回归法和偏最小二乘法比较 总被引:5,自引:1,他引:5
研究了主成分回归和偏最小二乘方法在多组分分光光度法分析中的应用,以5-Br-PADAP(2〔5-溴-2-吡啶)-偶氮〕5-二乙氨基苯酚)为显色剂,OP(聚乙二醇辛基苯基醚)作为增溶增稳剂,在pH=3.6的条件下,用主成分回归及偏最小二乘分光光度法同时测定了合成样中的铜、钴、镍、钒4组分含量,测定相对误差在-6.00%~4.00%之间。实验证明,对于加和性不好的体系偏最小二乘分光光度法要优于主成分回 相似文献
10.
11.
12.
含钒碳质页岩中钒的物相分析 总被引:2,自引:0,他引:2
将含钒碳质页岩经物相分离后 ,在浓度为 0 .75mol/ L H3 PO4介质中及 H2 O2 存在下 ,以 Na F、Cy DTA为掩蔽剂 ,5- Br- PADAP为显色剂 ,分别测定矿物各相中钒的含量。方法检出限为 2 .6× 1 0 -8mol/ L,RSD为4 .9% ( n=5) 相似文献
13.
六极杆碰撞反应池-等离子体质谱测定生物样品中痕量铬和钒 总被引:1,自引:0,他引:1
采用带六极杆碰撞反应池的电感耦合等离子体质谱直接测定了生物样品中痕量铬和钒。在碰撞反应池中引入He/NH3(93∶7)混合气,有效地消除了分子离子(ArC 、NCl 、Cl O 、Cl OH 等)对超痕量铬、钒测定的干扰,降低了方法的检出限。比较了干法灰化和湿法消解两种样品处理方法,两种消解方式获得的结果基本一致。方法的检出限(3σ):钒为0.005 0μg.g-1,铬为0.001 8μg.g-1。相对标准偏差:钒为3.25%~14.08%;铬为4.20%~8.24%。经国家一级生物标准物质验证,测定值与标准值吻合。 相似文献
14.
《Analytical letters》2012,45(13):999-1004
Abstract The spectrophotometric study of violet complex isophthaldihydroxamic acid-vanadium extracted into solution of trioctylmethylammonium chloride in ethylacetate was made (λmax = 380 nm, ? = 7500 l.mol?1.cm?1; λmax = 510 nm, ? = 5510 l.mol?1 .cm?1; stoichiometries, 1:1 and 1:2, V:reagent). A new method for the extract-spectrophotometric determination of V(V) in the range 14–80 μg of vanadium is proposed. 相似文献
15.
成勇 《理化检验(化学分册)》2012,(3):328-331
采用盐酸消解五氧化二钒样品及其中所含可溶性杂质,再以无水碳酸钾与硼酸高温熔融不可溶性杂质,然后以盐酸溶解熔块,合并溶液后以用电感耦合等离子体原子发射光谱法测定杂质元素铌、锆、钛、钨、硅、铝、钼、钴、铬、镍、铜、铅、镉、砷、磷、铁、锰、钙和镁的含量。试验了基体元素和共存元素对测定的干扰,优化各元素的分析谱线,运用同步背景校正消除基体影响。19种元素的检出限在10~225μg.L-1之间,背景等效浓度在5~150μg.L-1之间。方法用于分析五氧化二钒样品,测定结果与其它化学分析方法测定值一致;分析五氧化二钒标准样品(GSBH 42015-96)的测定值与标准值相一致。 相似文献
16.
钒(Ⅴ)-硫氰酸盐-碱性三芳基甲烷染料的显色反应研究 总被引:3,自引:0,他引:3
研究了在表面活性剂存在下,钒(V)与硫氰酸盐和结晶紫、孔雀绿、灿烂绿、甲基紫及维多利亚蓝4R等碱性三芳基甲烷染料形成离子缔合物的显色反应.讨论了钒(V)-硫氰酸盐-结晶紫-阿拉伯树胶体系的反应条件和分析特性。摩尔吸光系数为2.55×105L·mol-1·cm-1.此法可用于铝合金中微量钒的测定。 相似文献
17.
Krystyna Pyrzyńska 《Mikrochimica acta》2005,149(3-4):159-164
Owing to the toxic and essential nature of vanadium in biological systems, there has been considerable interest in the determination of its content in different kinds of samples. Among several analytical techniques for the determination of vanadium, spectrophotometric methods are very popular due to their simplicity and low-cost instrumentation. Various attempts have been made to modify these methods in order to improve their sensitivity and selectivity. This review shows recent developments in the spectrophotometric determination of vanadium and highlights those which can be used for speciation analysis of this element. 相似文献
18.
本文报道钒渣中测定二氧化钛的硫酸高铈容量法,在盐酸-硫酸混酸介质中,控制磷酸浓度大于3.5mol/L,在用铝片还原Ti(Ⅳ)时可以消除大量钒的干扰,方法用于实际试样分析,结果较好。 相似文献
19.
20.
《Analytical letters》2012,45(4):187-196
Abstract Trace amounts of vanadium catalyze the oxidation of phenylhydrazine-p-sulfonic acid by sodium chlorate. The diazonium salt produced is coupled with 1-naphthylamine to form an azodyestuff whose absorbance is read at 530 nm. Interferences ate eliminated by separating the vanadium by solvent extraction. Physiological concentrations of vanadium are determined in 10 ml. of ashed human blood or plasma and 25 ml. of ashed human urine. Recovery studies are reported along with results for the analysis of blood and urine samples. 相似文献