Table 3.
S. number | Analyte | Analytical instrument used for the detection | Method | Limit of detection (LOD)# | Linearity range | Analyzed samples | Interference study | Supporting media | Reference |
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1 | Hg(II) | DP-ASV | Electrochemical | 4.99 × 10−8 M | — | Ambient water, tap, and wastewaters | Palladium-natural phosphate-carbon paste electrode enhances the selectivity for Hg2+ | Natural phosphate electrodes | [103] |
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2 | Hg(II) | SW-ASV | Electrochemical | 0.04 × 10−6 M | 0.2–10.0 μM | Foodstuffs | Simultaneously both Cd2+ and Hg2+ are determined and 1,000-fold for K+, Na+, Li+, NH4 +, Ca2+, Mg2+, Pb2+, Zn2+, Cr3+, Fe2+, Co2+, and Al3+ did not interfere | Carbon paste electrode | [104] |
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3 | Hg(II) | Differential pulse voltammeter | Electrochemical | 4.48 × 10−10 M | 0.2–10 μg L−1 | Spiked fish and plant samples | Cu(II), Mg(II), As(III), and Cr(II) were possible interferers | 4,4′-Bipyridine-silver polymer | [105] |
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4 | Hg(II) | Cyclic voltammeter | Electrochemical | 0.8 × 10−14 M | 10−14–10−7 M | — | Cu2+, Pb2+, Ni2+, Zn2+, Cr3+, Co3+, As5+, Fe2+, and Fe3+ did not interfere | Gold atomic cluster-chitosan | [106] |
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5 | Hg(II) | Voltammeter (cyclic and differential pulse) |
Biosensor | 3.93 × 10−12 M | 0.005–0.034 mM | Water samples | The working potential controlled to minimize the interference of other metal ions in test medium | PANI and PANI-co-PDTDA polymer films | [107] |
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6 | Hg(II) | ASV | Electrochemical | 4.98 × 10−9 M | 4–160 ppb | Aquatic solutions | — | Glassy carbon electrode | [108] |
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7 | Hg(II) | SW-ASV | Electrochemical | 9.2 × 10−5 M | 0.1–150.0 nM | Soil, gasoline, fish, tap, and wastewaters | 400-fold mass ratio of Cu2+, Mn2+, Zn2+, Cr3+, Cr6+, Fe3+, Fe2+, Ni2+, and Co2+ did not interfere in the simultaneous determination of Cd2+, Pb2+, and Hg2+ | Triphenyl phosphine | [109] |
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8 | Hg(II) | Potentiometer | Electrochemical | 9.77 × 10−6 M (PME)1
7.76 × 10−7 M (CGE)1 |
1.0 × 10−1–5.0 × 10−6 M (PME) 1.0 × 10−1–5.0 × 10−7 M (CGE) |
Water samples | Ag+ has small interference in the determination of Hg2+ | 1,3-Alternate thiacalix[4]crown | [110] |
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9 | Hg(II) | Potentiometer | Electrochemical | 1.0 × 10−8 M | 5.0 × 10−8–1.0 × 10−2 M | — | The selectivity coefficient of the other ions is ranging from 2.9 to 4.9 | PVC membrane | [111] |
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10 | Hg(II) | DPSV | Electrochemical | 0.05 × 10−12 M | 1–500 nM | Water samples | Pb2+, Th3+, Cu2+, Cd2+, Ni2+, and Al3+ did not interfere | Gold nanoparticles | [112] |
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11 | Hg(II) | SW-ASV | Ultrasonic extraction | — | — | Indoor dust samples | — | Gold nanoparticles | [113] |
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12 | Hg(II) | Cyclic voltammeter | Electrochemical | 1.9 × 10−9 M | 40–170 μg L−1 | Wastewaters | — | Biotinyl Somatostatin-14 peptide | [114] |
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13 | Hg(II) | Potentiometer | Electrochemical | 3 × 10−6 M | 5 × 10−6–1 × 10−2 M | Contaminated water | Na+, K+, Mg2+, Ca2+, Zn2+, Cu2+, Cr3+, Fe3+, and Pb2+ did not interfere in the determination of Hg2+ | Dithizone and di-n-butyl phthalate | [115] |
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14 | Hg(II) | DP-ASV | Electrochemical | 0.483 × 10−6 M | 300–700 ng mL−1 | — | No interference of Cd, Ni, Zn, and Cu in 50-, 25-, 100-, and 5-fold in excess, respectively | Nanocellulosic fibers | [116] |
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15 | Hg(II) | — | Electrochemical | 0.5 × 10−9 M | 1.0 nM–1.0 μM | Zn2+, Mg2+, Ca2+, Pb2+, Cd2+, Mn2+, Cu2+, Ni2+, and Fe3+ did not interfere | G-quadruplex–hemin (G4–hemin) | [117] |
#For the conversion of limit of detection values into moles per liter (M) the atomic weight of Hg is taken as 200.59 g, MeHg as 215.59 g, EtHg as 229.59 g, and PhHg as 277.59 g.
1PME: polymeric membrane electrode and CGE: coated graphite electrode.
Analytical instruments: DP-ASV: differential pulse anodic stripping voltammeter; SW-ASV: square wave anodic stripping voltammeter.