Research output: Contribution to journal › Article › peer-review
Reversed-phase chromatomembrane extraction as a novel approach for automated sample pretreatment : Anions determination in biodiesel by ion chromatography with conductivity detection. / Shishov, Andrey; Stolarova, Elena; Moskvin, Leonid; Bulatov, Andrey.
In: Analytica Chimica Acta, Vol. 1087, 09.12.2019, p. 62-68.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Reversed-phase chromatomembrane extraction as a novel approach for automated sample pretreatment
T2 - Anions determination in biodiesel by ion chromatography with conductivity detection
AU - Shishov, Andrey
AU - Stolarova, Elena
AU - Moskvin, Leonid
AU - Bulatov, Andrey
PY - 2019/12/9
Y1 - 2019/12/9
N2 - In this study, a reversed-phase chromatomembrane extraction (RP-CME) method as a novel approach for automated sample pretreatment was suggested for the first time. The RP-CME was applied to automated separation of anions (formate, chloride, nitrate, phosphate and sulfate) from biodiesel samples as a proof-of-concept example. The novel design of chromatomembrane cell was developed for on-line RP-CME. The RP-CME procedure assumed mass-transfer of water-soluble analytes from organic sample phase (biodiesel sample) to aqueous phase supported in a porous composite mass-transfer block. The composite mass-transfer block based on microporous hydrophobic poly (tetrafluoroethylene) and hydrophilic glass fiber was developed for the RP-CME implementation. The block provided the effective retention of aqueous phase into the cell and simultaneous penetration of organic phase. The hydrophilic membrane-based sheet was used for the on-line separation of hydrophilic emulsion (biodiesel in water) containing target analytes obtained during analytes elution by aqueous phase from the mass-transfer block. The RP-CME was successfully coupled with an ion chromatography with conductivity detection. The limits of detection, calculated from a blank test based on 3σ, were 5 μg kg−1 for sulfate, 6 μg kg−1 for nitrate, 3 μg kg−1 for chloride, 5 μg kg−1 for phosphate and 1 μg kg−1 for formate.
AB - In this study, a reversed-phase chromatomembrane extraction (RP-CME) method as a novel approach for automated sample pretreatment was suggested for the first time. The RP-CME was applied to automated separation of anions (formate, chloride, nitrate, phosphate and sulfate) from biodiesel samples as a proof-of-concept example. The novel design of chromatomembrane cell was developed for on-line RP-CME. The RP-CME procedure assumed mass-transfer of water-soluble analytes from organic sample phase (biodiesel sample) to aqueous phase supported in a porous composite mass-transfer block. The composite mass-transfer block based on microporous hydrophobic poly (tetrafluoroethylene) and hydrophilic glass fiber was developed for the RP-CME implementation. The block provided the effective retention of aqueous phase into the cell and simultaneous penetration of organic phase. The hydrophilic membrane-based sheet was used for the on-line separation of hydrophilic emulsion (biodiesel in water) containing target analytes obtained during analytes elution by aqueous phase from the mass-transfer block. The RP-CME was successfully coupled with an ion chromatography with conductivity detection. The limits of detection, calculated from a blank test based on 3σ, were 5 μg kg−1 for sulfate, 6 μg kg−1 for nitrate, 3 μg kg−1 for chloride, 5 μg kg−1 for phosphate and 1 μg kg−1 for formate.
KW - Anions
KW - Automated sample pretreatment
KW - Biodiesel
KW - Chromatomembrane cell
KW - Ion chromatography with conductivity detection
KW - Reversed-phase chromatomembrane extraction
KW - ONLINE COLLECTION/CONCENTRATION
KW - TRACE AMOUNTS
KW - METHANOL
KW - GLYCEROL
KW - DIOXIDE
KW - AIR
KW - FLOW
KW - CHEMISTRY
KW - SEPARATION
KW - CELL
UR - http://www.scopus.com/inward/record.url?scp=85071247228&partnerID=8YFLogxK
UR - http://www.mendeley.com/research/reversedphase-chromatomembrane-extraction-novel-approach-automated-sample-pretreatment-anions-determ
U2 - 10.1016/j.aca.2019.08.031
DO - 10.1016/j.aca.2019.08.031
M3 - Article
AN - SCOPUS:85071247228
VL - 1087
SP - 62
EP - 68
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
SN - 0003-2670
ER -
ID: 46161342