Table 1.
Analyte(s) | Sample | Reaction | Sampling Rate (h−1) | CV (%) | Remarks | Ref. |
---|---|---|---|---|---|---|
Acetaminophen or isoxsuprine, isoniazid | Pharmaceuticals | Reaction with 1-fluoro-2,4-dinitrobenzene releasing fluoride | 40 | 1.8–3.6 | Detection by a fluoride ion-selective electrode | [92] |
Ascorbic acid, cysteine | Dietary supplements | Reduction of 8-molybdodiphosphate | ― | 1.3–3.2 | Novel approach for data treatment (mean centering of ratio kinetic profiles method) | [93] |
Bromate, chlorite | Treated water | Analytes oxide bromide reagent to bromine, which reacts with o-dianisidine | ― | 8.5–8.8 | Sample splitting, reaction at different temperatures | [77] |
Bromide | Brine | Bromide oxidation by chloramine T, reaction with phenol red | 60 | <1.0 | Slower reaction with chloride minimising its interference | [94] |
Carbofuran, propoxur, metolcarb, fenobucarb | Water, fruits | Hydrolysis/diazotization with p-nitroaniline in alkaline medium | 18 | 0.8–3.3 | Data processing by back-propagation/artificial neural network | [95] |
Cathecol, resorcinol | Synthetic mixtures | Oxidation by H2O2 under peroxidase catalysis | 60 | 3.4 | Flow stopping associated to multiple linear regression | [82] |
Chlorpyrifos, carbaryl | Pesticide formulations | Oxidation by H2O2 under alkaline medium | 80 | 4.0–6.0 | Exploitation of different analytes degradation rates | [83] |
Cobalt, nickel | Synthetic mixtures | Complexation with HBAT | ― | ― | Different strategies to modify the sample residence times | [84] |
Cobalt, nickel | Metal alloys | Complexation with PAR from citrate complexes | 40 | <1.0 | Relocatable reactor to achieve two sample residence times | [80] |
Copper, nickel | Plant materials | Complexation with Br-PADAP | 20 | 2.0 | Relocation of the flow cell for detection at two sample residence times | [81] |
Free and total SO2 | Wines | p-rosaniline method | 55 | <3.1 | Dual flow stopping, measurements before and after alkaline hydrolysis | [85] |
Furfural, vanillin | Synthetic mixtures | Reactions with p-aminophenol, yielding Shiff bases | 30 | 0.2–1.9 | Zone splitting to achieve two sample residence times | [78] |
Gallium, aluminum | Synthetic mixtures | Complexation with PAR | ― | 0.8–1.6 | Flow stopping, principal component regression | [86] |
Glucose, fructose | Synthetic mixtures | Analytes oxidation by periodate | ― | 2.0 | Remaning periodate detected by reaction with pyrogallol | [87] |
3-Hydroxybutyrate, 3-hydroxyvalerate | Biodegraded polymers | 3-hydroxybutyrate dehydrogenase-catalysed reaction with coenzyme NAD+ |
20 | 0.8–1.5 | Exploitation of differential enzimatic reactions with two enzyme reactors and fluorimetric/spectrophotometric detectors placed in series | [79] |
Iron, copper | Wastewater, pharmaceuticals | Hydroxylamine oxidation yielding nitrite, determined by Griess method | 32–39 | 1.3–1.6 | Microchip with two reaction coils at different temperatures | [88] |
Iron, vanadium | Metal alloys | Iodide oxidation by Cr(VI) | 50 | 0.5–3.0 | Differential catalitic effect, data treatment by PLS | [23] |
Levodopa, benserazide | Pharmaceutical formulations | Analytes oxidation by periodate | 20 | 2.5–4.0 | Flow stopping, multiway PLS | [89] |
Molybdate, tungstate | Steels | Iodide oxidation by H2O2 | ― | 1.6–3.4 | Mathematical algorithm to compensate the synergistic analytes catalytic effects | [90] |
Phosphate, silicate | Waters | Oxidation of thiamine to thiochrome by the molybdate heteropoly acids | 60 | 0.25–0.7 | Exploitation of different rates of the molybdate heteropoly acids formation | [91] |
Br-PADAP: 2-(5-bromo-2-pyridylazo)-5-(diethylamino)-phenol; HBAT: 2-hydroxybenzaldehyde thiosemicarbazone; NAD+: Nicotinamide adenine dinucleotide; PAR: 4-(2-pyridylazo) resorcinol; PLS: Partial least squares regression.