- Title
- Smartphone app-based/portable sensor for the detection of fluoro-surfactant PFOA
- Creator
- Fang, Cheng; Zhang, Xiang; Dong, Zhaomin; Wang, Liang; Megharaj, Mallavarapu; Naidu, Ravi
- Relation
- Chemosphere Vol. 191, Issue January 2018, p. 381-388
- Publisher Link
- http://dx.doi.org/10.1016/j.chemosphere.2017.10.057
- Publisher
- Elsevier
- Resource Type
- journal article
- Date
- 2018
- Description
- We developed a smartphone app-based monitoring tool for the detection of anionic surfactants (AS), including perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS). Akin to the methylene blue active substances (MBAS), liquid-phase extraction (LPE) is employed to extract the hydrophobic ion-pair of dye (ethyl violet)-AS to an organic phase (ethyl acetate). The colour (RGB) of the organic phase is read using a smartphone camera with the help of a reading kit. The value of RGB is carefully corrected and linked to the concentration of ASs with a standard deviation of <10% in the 10–1000 ppb (part per billion) range. In order to avoid the interference arising from inorganic anions (such as those found in tap water and groundwater), the water sample is pre-treated either by solid-phase extraction (SPE), which takes ∼30 min, or by dual liquid-phase extraction (dual-LPE, developed by us), which takes ∼5 min. In the latter case, the organic phase of the first LPE (equilibrium with water sample) is transferred and subjected to a second LPE (equilibrium with Milli-Q water) to remove any potential background interference. In the meantime, SPE can also pre-concentrate ASs at 100–1000 times (in volume) to benefit the sensitivity. Consequently, our smartphone app can detect PFOA spiked in tap/groundwater with an LOD of 10 ppb (∼12 nM, dual-LPE of ∼5 min), or 0.5 ppb (∼1.2 nM, SPE of ∼3 h), suggesting that it has the potential to succeed as a pre-screening tool for on-site application and in common laboratory tests.
- Subject
- smartphone app; fluoro-surfactant; PFOA; pre-screening tool; on-site; dual-LPE
- Identifier
- http://hdl.handle.net/1959.13/1350552
- Identifier
- uon:30570
- Identifier
- ISSN:0045-6535
- Language
- eng
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