Coprecipitation with lanthanum phosphate as a technique for separation and preconcentration of iron(III) and lead

被引:29
作者
Kagaya, S [1 ]
Saiki, M [1 ]
Malek, ZA [1 ]
Araki, Y [1 ]
Hasegawa, K [1 ]
机构
[1] Toyama Univ, Fac Engn, Dept Chem & Biochem Engn, Toyama 9308555, Japan
来源
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY | 2001年 / 371卷 / 03期
关键词
D O I
10.1007/s002160100976
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The usefulness of coprecipitation with lanthanum phosphate for separation and preconcentration of some heavy metals has been investigated. Although lanthanum phosphate coprecipitates iron(III) and lead quantitatively at pH 2.3, iron(H) can barely be collected at this pH. This coprecipitation technique was applicable to the separation and preconcentration of iron(III) before inductively coupled plasma atomic-emission spectrometric (ICP-AES) determination; the recoveries of iron(III) and iron(II) from spiked water samples were 103-105% and 0.2-0.7%, respectively. The coprecipitation was also useful for separation of 20 mug lead from 100 mL of an aqueous solution that also contained 1-100 mg iron. Coprecipitation of iron was substantially suppressed by addition of ascorbic acid, which enabled recovery of 97-103% of lead added to the solution, bringing the recovery to within 1.6-5.0% of the relative standard deviations. Lanthanum phosphate can also coprecipitate cadmium and indium quantitatively, although chromium(III), cobalt, and nickel and large amounts of sodium, potassium, magnesium, and calcium are barely coprecipitated at pH 3.
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页码:391 / 393
页数:3
相关论文
共 15 条
[1]  
Alfasi Z.B., 1992, Preconcentration Techniques for Trace Elements, P33
[2]   Analysis of geological materials for bismuth, antimony, selenium and tellurium by continuous flow hydride generation inductively coupled plasma mass spectrometry .2. Methodology and results [J].
Hall, GEM ;
Pelchat, JC .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1997, 12 (01) :103-106
[3]  
KIM YS, 1995, B KOR CHEM SOC, V16, P582
[4]   SIMULTANEOUS DETERMINATION OF 7 TRACE IMPURITIES (AL, AS, CR, FE, TI, V AND ZR) AND HIGH-PURITY NICKEL METAL AND NICKEL-OXIDE BY COPRECIPITATION AND INDUCTIVELY-COUPLED PLASMA-ATOMIC EMISSION-SPECTROMETRY [J].
KUJIRAI, O ;
YAMADA, K .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1994, 348 (11) :719-723
[5]  
Kujirai O, 1996, FRESEN J ANAL CHEM, V354, P428
[6]  
MARCZENKO Z, 1963, CHEM ANAL, V7, P775
[7]  
MERCZENKO Z, 1964, CHIM ANAL-PARIS, V46, P286
[8]  
Mizuike A., 1983, ENRICHMENT TECHNIQUE, P56
[9]   Determination of ultra-trace amounts of selenium (IV) by flow injection hydride generation atomic absorption spectrometry with on-line preconcentration by co-precipitation with lanthanum hydroxide .2. On-line addition of co-precipitating agent [J].
Nielsen, S ;
Sloth, JJ ;
Hansen, EH .
ANALYST, 1996, 121 (01) :31-35
[10]   LANTHANUM COPRECIPITATION METHOD FOR THE DETERMINATION OF SELENIUM IN ENVIRONMENTAL WATER [J].
SAISHO, H ;
FUJIMURA, Y .
ANALYTICAL SCIENCES, 1990, 6 (04) :619-621