Simple Colorimetric Analysis for Determining Hexavalent Chromium with High Sensitivity via Homogeneous Liquid-Liquid Extraction

被引:6
|
作者
Yokota, Yuki [1 ]
Manaka, Atsushi [2 ]
Tafu, Masamoto [2 ]
Kato, Takeshi [3 ]
Tomita, Keiichi [4 ]
Akazawa, Toshiyuki [4 ]
机构
[1] Toyama Coll, Natl Inst Technol, Adv Course, 13 Hongo, Toyama 9398630, Japan
[2] Toyama Coll, Dept Appl Chem & Chem Engn, Natl Inst Technol, 13 Hongo, Toyama 9398630, Japan
[3] Ind Technol Innovat Ctr Ibaraki Prefecture, Tsukuba, Ibaraki 3113195, Japan
[4] Hokkaido Res Org, Ind Res Inst, Sapporo, Hokkaido 0600819, Japan
关键词
Phase separation; Hexavalent chromium; Water/2-propanol/dimethyl phthalate; SEPARATION;
D O I
10.1246/bcsj.20180351
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Colorimetric analysis with diphenylcarbazide has been used as a simple method to determine hexavalent chromium (Cr(VI)). However, the low sensitivity of this technique makes it difficult to determine concentrations close to the environmental standard value (0.05 mg/L). We found that the phase separation phenomenon produced a small amount of the extraction phase when a mixture of 2-propanol and a small amount of dimethyl phthalate were added to a water sample, and that the Cr(VI)-diphenylcarbazide complex was extracted into this phase with high efficiency. Based on these findings, we report a simple method for colorimetric analysis for determining Cr(VI) with high sensitivity via homogeneous liquid-liquid extraction using water, 2-propanol, and dimethyl phthalate. As a result, the extraction percentage for Cr(VI) was 88% and the concentration factor improved up to 121-fold (27.4 mL -> 226 mu L). Using the proposed extraction method, determination limit (10 sigma) and detection limit (3 sigma) were 0.11 ppb and 0.03 ppb, respectively. This method can be employed for the determination of hexavalent chromium in groundwater systems by the use of EDTA as masking agent.
引用
收藏
页码:807 / 810
页数:4
相关论文
共 50 条
  • [1] Simple colorimetric analysis for determining hexavalent chromiumwith high sensitivity via homogeneous liquid-liquid extraction
    Yokota, Yuki
    Manaka, Atsushi
    Tafu, Masamoto
    Kato, Takeshi
    Tomita, Keiichi
    Akazawa, Toshiyuki
    Bulletin of the Chemical Society of Japan, 2019, 92 (04): : 807 - 810
  • [2] Simple and high-sensitivity colorimetric analysis of cadmium using homogeneous liquid-liquid extraction
    Manaka, Atsushi
    Ueno, Yumemi
    Tafu, Masamoto
    Kato, Takeshi
    ANALYTICAL SCIENCES, 2022, 38 (01) : 223 - 226
  • [3] Simple and high-sensitivity colorimetric analysis of cadmium using homogeneous liquid–liquid extraction
    Atsushi Manaka
    Yumemi Ueno
    Masamoto Tafu
    Takeshi Kato
    Analytical Sciences, 2022, 38 : 223 - 226
  • [4] Speciation of hexavalent chromium in waters by liquid-liquid extraction and GFAAS determination
    Beni, Aron
    Karosi, Roland
    Posta, Jozsef
    MICROCHEMICAL JOURNAL, 2007, 85 (01) : 103 - 108
  • [5] Hexavalent chromium extraction from aqueous solutions in a liquid-liquid slug flow microreactor
    Sattari-Najafabadi, Mehdi
    Esfahany, Mohsen Nasr
    CHEMICAL ENGINEERING AND PROCESSING-PROCESS INTENSIFICATION, 2020, 157
  • [6] Hexavalent Chromium Recovery by Liquid-Liquid Extraction with Tributylphosphate from Acidic Chloride Media
    A. Ouejhani
    M. Dachraoui
    G. Lalleve
    J. F. Fauvarque
    Analytical Sciences, 2003, 19 : 1499 - 1504
  • [7] Hexavalent chromium recovery by liquid-liquid extraction with tributylphosphate from acidic chloride media
    Ouejhani, A
    Dachraoui, M
    Lalleve, G
    Fauvarque, JF
    ANALYTICAL SCIENCES, 2003, 19 (11) : 1499 - 1504
  • [8] Development of High Sensitive Smart Device Analysis with Homogeneous Liquid-Liquid Extraction
    Manaka, Atsushi
    Yokota, Yuki
    Kato, Takeshi
    Shibata, Yoshiyuki
    Tafu, Masamoto
    BUNSEKI KAGAKU, 2019, 68 (06) : 411 - 415
  • [9] Mechanism of homogeneous liquid-liquid extraction
    Kao Teng Hsueh Hsiao Hua Heush Hsueh Pao, 5 Suppl (236):
  • [10] SIMPLE LIQUID-LIQUID EXTRACTION APPARATUS
    DOERING, CH
    TARVER, H
    ANALYTICAL BIOCHEMISTRY, 1964, 9 (04) : 498 - &