首页> 外文期刊>Journal of AOAC International >Speciation of selenium in environmental samples by solid-phase spectrophotometry using 2,3-dichloro-6-(2,7-dihydroxy-naphthylazo)quinoxaline.
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Speciation of selenium in environmental samples by solid-phase spectrophotometry using 2,3-dichloro-6-(2,7-dihydroxy-naphthylazo)quinoxaline.

机译:使用2,3-二氯-6-(2,7-二羟基萘基偶氮)喹喔啉的固相分光光度法测定环境样品中的硒形态。

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摘要

Solid-phase spectrophotometry was applied to determination of trace amounts of selenium (Se) in water, soil, plant materials, human hair, and a cosmetic preparation (lipstick). Se(IV) was sorbed in a dextran type lipophilic gel as a complex with 2,3-dichloro-6-(2,7-dihydroxy-naphthylazo)quinoxaline (DCDHNAQ), whereas Se(VI) was determined after boiling in HCl for 10 min to convert Se(VI) to Se(IV). Resin phase absorbances at 588 and 800 nm were measured directly, which allowed the determination of Se in the range of 0.2-3.3 micro g/L with an RSD of 1.22%. The influences of analytical parameters including pH of the aqueous solution, amounts of DCDHNAQ, and sample volume were investigated. The molar absorptivities were found to be 1.09x106, 4.60x106, and 1.23x107 L/mol cm for 100, 500, and 1000 mL, respectively. The LOD and LOQ of the 500 mL sample method were 110 and 360 ng/L, respectively, when using 50 mg dextran type lipophilic gel. For a 1000 mL sample, the LOD and LOQ were 60 and 200 ng/L, respectively, using 50 mg of the exchanger. Increasing the sample volume enhanced the sensitivity. No considerable interferences were observed from other investigated anions and cations on the Se determination.
机译:固相分光光度法用于测定水,土壤,植物材料,人发和化妆品(唇膏)中的痕量硒(Se)。 Se(IV)与2,3-dichloro-6-(2,7-dihydroxy-naphthylazoazoazo)quinoxaline(DCDHNAQ)形成复合物,被吸附在葡聚糖型亲脂性凝胶中,而在HCl中沸腾10分钟将Se(VI)转换为Se(IV)。直接测量在588和800 nm处的树脂相吸光度,从而可以在0.2-3.3 micro g / L范围内测定Se,RSD为1.22%。研究了分析参数对水溶液pH值,DCDHNAQ量和样品量的影响。发现100、500和100摩尔摩尔吸收率分别为1.09x10 6 ,4.60x10 6 和1.23x10 7 L / mol cm。分别为1000 mL。当使用50 mg葡聚糖型亲脂性凝胶时,500 mL样品方法的LOD和LOQ分别为110和360 ng / L。对于1000 mL样品,使用50 mg的交换剂,LOD和LOQ分别为60和200 ng / L。增加样品量可提高灵敏度。在测定硒时,没有观察到其他阴离子和阳离子的明显干扰。

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