Cathodic Stripping Voltammetric Study for Determination of Inorganic Arsenic Species in Seaweed Gracilaria fisheri

2019 ◽  
Vol 886 ◽  
pp. 78-85
Author(s):  
Charuwan Khamkaew ◽  
Lalitporn Wongsuwan ◽  
Abdullateep Sareedeh

A simple, rapid, selective and sensitive square wave cathodic stripping voltammetry (SWCSV) at a hanging mercury drop electrode (HMDE) for the determination of As(III), As(V) and inorganic As(total) in seaweed was developed. The method was based on the formation of copper-arsenic intermetallic compound in the presence of HCl onto a HMDE at a constant potential of -0.40 V vs. Ag/AgCl in the deposition step, followed by the reduction of deposited compound to arsine at a potential of -0.78 V in the stripping step. In the system, only As(III) was directly measured, whereas inorganic As(total) was measured by reducing As(V) to As(III) using thiosulfate. In the deposition step, the use of 10 mg L-1 Cu(II) and 1 M HCl was recommended for the determination of 2 µg L-1 As(III) under the optimum instrumental variables obtained at 150 s for deposition time and 2000 rpm for stirring speed with the highest deposition efficiency of 16.15 and 88.49%, respectively. In the determination of As(V), two values of the highest reduction efficiency obtained using concentration of 40 mg L-1 thiosulfate, and reducing time at 300 s were 98.15% and 37.89%, respectively. In the measurement, the quantification limits of As(III) and As(V) were 0.46, and 1.62 µg L-1, respectively. The relative standard deviation (n=10) for 2 ug L-1 As(III) and As(V) were 5.20% and 2.57%, respectively. The proposed method was applied to the determination of inorganic arsenic species in seaweed Gracilaria fisheri.

2016 ◽  
Vol 71 (8) ◽  
pp. 823-833 ◽  
Author(s):  
E. A. Zakharova ◽  
S. G. Antonova ◽  
G. N. Noskova ◽  
L. N. Skvortsova ◽  
A. V. Te

1976 ◽  
Vol 59 (3) ◽  
pp. 650-654 ◽  
Author(s):  
Walter Holak

Abstract Arsenic and selenium are determined in foods by differential pulse polarography and cathodic stripping voltammetry. The sample is digested with nitric acid and magnesium nitrate and then dissolved in dilute hydrochloric acid. An aliquot is removed, the arsenic is chemically reduced to the trivalent state, and interferences are removed by ion exchange before polarography. Selenium is determined in a second aliquot by cathodic stripping voltammetry. Recoveries for both elements in several foods were from 90 to 110%. The relative standard deviations for arsenic at 5 ppm and selenium at 0.48 ppm were 5.8 and 7.3%, respectively.


2001 ◽  
Vol 16 (7) ◽  
pp. 762-766 ◽  
Author(s):  
Amparo Martinez ◽  
Angel Morales-Rubio ◽  
M. Luisa Cervera ◽  
Miguel de la Guardia

2010 ◽  
Vol 673 (2) ◽  
pp. 185-193 ◽  
Author(s):  
Nureddin Ben Issa ◽  
Vladana N. Rajaković-Ognjanović ◽  
Branislava M. Jovanović ◽  
Ljubinka V. Rajaković

2006 ◽  
Vol 6 (6) ◽  
pp. 175-182 ◽  
Author(s):  
G.J. Liu ◽  
X.R. Zhang ◽  
J. Jain ◽  
J.W. Talley ◽  
C.R. Neal

Effect of natural organic matter (NOM) on the stability of inorganic arsenic species in simulated raw water was examined at circumneutral pH. An ion chromatography–inductively coupled plasma mass spectrometry system was used for simultaneous determination of As(III) and As(V). A reduction of arsenate (As(V)) to arsenite (As(III)) was observed in the unfiltered simulated raw waters (USW). The As(V) reduction to As(III) did not occur in the simulated waters that passed through a 0.2 μm membrane (FSW). Microorganism activities is probably the major reason causing As(V) reduction in the USW. In the FSW without NOM, As(III) tended to be oxidized into As(V). The addition of 0.036 mM of Fe(II) significantly facilitated the oxidation. The presence of 10 mg/L Suwannee River NOM as C inhibited As(III) oxidation no matter whether Fe(II) existed or not. The experimental results suggest that NOM can mediate distribution of inorganic arsenic species in water, thus it is an important factor controlling the mobility and toxicity of arsenic in drinking water.


2012 ◽  
Vol 77 (6) ◽  
pp. 775-788 ◽  
Author(s):  
Issa Ben ◽  
Aleksandar Marinkovic ◽  
Ljubinka Rajakovic

A simple and efficient method for separation and determination of dimethylarsenate DMAs(V) was developed in this work. Two resins, a strong base anion exchange (SBAE) resin and iron-oxide coated hybrid (HY) resin were tested. By simple adjusting pH value of water at 7.00, DMAs(V) passed through the HY column without any changes, while all other arsenic species [inorganic arsenic and monomethylarsonate, MMAs(V)] were quantitatively bonded on HY resin. The resin capacity was calculated according to the breakthrough points in a fixed bed flow system. At pH 7.00 the HY resins bonded more than 4150 ?g g-1 of As(III), 3500 ?g g-1 of As(V) and 1500 ?g g1 of MMAs(V). Arsenic adsorption behavior in the presence of impurities showed tolerance with the respect to potential interference of anions commonly found in natural water. DMAs(V) was determined in the effluent by ICP-MS. The detection limit was 0.03 ?g L?1 and relative standard deviation (RSD) was between 1.1?7.5 %. Proposed method was established performing standard procedures: with external standard, certified reference material and the standard addition method.


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