scholarly journals Simple and Equipment-Free Paper-Based Device for Determination of Mercury in Contaminated Soil

Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 2004
Author(s):  
Hikmanita Lisan Nashukha ◽  
Jirayu Sitanurak ◽  
Hermin Sulistyarti ◽  
Duangjai Nacapricha ◽  
Kanchana Uraisin

This work presents a simple and innovative protocol employing a microfluidic paper-based analytical device (µPAD) for equipment-free determination of mercury. In this method, mercury (II) forms an ionic-association complex of tetraiodomercurate (II) ion (HgI42−(aq)) using a known excess amount of iodide. The residual iodide flows by capillary action into a second region of the paper where it is converted to iodine by pre-deposited iodate to liberate I2(g) under acidic condition. Iodine vapor diffuses across the spacer region of the µPAD to form a purple colored of tri-iodide starch complex in a detection zone located in a separate layer of the µPAD. The digital image of the complex is analyzed using ImageJ software. The method has a linear calibration range of 50–350 mg L−1 Hg with the detection limit of 20 mg L−1. The method was successfully applied to the determination of mercury in contaminated soil and water samples which the results agreed well with the ICP-MS method. Three soil samples were highly contaminated with mercury above the acceptable WHO limits (0.05 mg kg−1). To the best of our knowledge, this is the first colorimetric µPAD method that is applicable for soil samples including mercury contaminated soils from gold mining areas.

2015 ◽  
Vol 8 ◽  
pp. ASWR.S22465 ◽  
Author(s):  
Diane Saint-Laurent ◽  
Francis Baril ◽  
Ilias Bazier ◽  
Vernhar Gervais-Beaulac ◽  
Camille Chapados

This research combines a hydrological and pedological approach to better understand the spatial distribution of contaminated soils along the Massawippi River (southern Québec, Canada). This river crosses through former mines, which were some of the largest copper mining areas in North America from 1865 to 1939. To determine the spatial distribution and concentration of the metal elements, soil samples were taken in each flood recurrence zone appearing on official flood zone maps. The maximum values obtained for Cu and Pb are 380 and 200 mg kg−1, respectively, for the soils in the frequent flood zones (FFzs), while the values for soils in the moderate flood zones (MFzs) range from 700 to 540 (Cu) and 580 to 460 mg kg−1 (Pb). Contamination extends through several kilometers of the former mining sites (Eustis and Capleton), and concentration of metals in alluvial soils is slightly higher near the mine sites.


2018 ◽  
Vol 33 (6) ◽  
pp. 1081-1085 ◽  
Author(s):  
Takeshi Ohno ◽  
Mutsumi Hirono ◽  
Shinichiro Kakuta ◽  
Shuhei Sakata

The determination of 90Sr by triple quadrupole ICP-MS is capable of providing a high sample throughput compared with radiometric analytical methods.


Author(s):  
M. Jamaluddin Ahmed ◽  
M. Tazul Islam ◽  
Sumaira Aziz

A very simple, ultra-sensitive and highly selective non-extractive spectrophotometric method for the determination of trace amounts of lead using 5,7-dibromo-8-hydroxyquinoline (DBHQ) has been developed. DBHQ reacts in a slightly acidic (0.0006-0.0025 M HCl) aqueous solution with lead (II) in 30% ethanolic media to produce highly absorbent a greenish-yellow chelate which has an absorption maximum at 390 nm. The reaction is instantaneous and the absorbance remains stable for over 24 h. The average molar absorption co-efficient and Sandal’s sensitivity were found to be 6.16 x 105 L mol-1cm-1 and 5 ng cm-2 of lead (II), respectively. Linear calibration graphs were obtained for 0.01- 60.0 mg L-1 of lead (II) having detection limit of 1.0 μg L-1 and RSD 0-2%. The stoichiometric composition of the chelate is 1:2 (Pb: DBHQ). A large excess of over 60 cations, anions and complexing agents (like, chloride, phosphate, azide, tartrate, oxalate, SCN- etc.) do not interfere in the determination. The developed method was successfully used in the determination of lead levels in several Standard Reference Materials (alloys, steels, natural water, bovine liver, human urine and hair) as well as in some environmental waters (potable and polluted), biological samples (human blood, urine and hair), soil samples, food samples (vegetables, rice, wheat) solutions containing both lead (II) and lead (IV) and complex synthetic mixtures. The results of biological and food analyses by the spectrophotometric method were found to be in excellent agreement with those obtained by AAS.


2019 ◽  
Vol 7 (5) ◽  
pp. 13-22 ◽  
Author(s):  
Hilary Uguru ◽  
Akpokodje, O. I.

This study was carried out to investigate the effect of compost manure and organic soap on hydrocarbon degradation in petroleum products contaminated soil. 10 kg of top soil collected at a depth of 0-20 cm, air dried and sieved, were poured into plastic containers. The soil samples were was pounded with 1 L of spent engine oil, 1 L of kerosene, 1 L of petrol and 1 L of diesel daily for five days. The containers were placed under natural environmental conditions for three weeks to enable full acclimatization of the petroleum products with the soil. A completely randomized design comprising T1 (Polluted soil without treatment ‘control’); T2 (10 kg contaminated soil + 500 g organic soap); T3 (10 kg contaminated soil + 500 g compost manure); and T4 (10 kg contaminated soil + 500 g compost manure + 500 g organic soap) was used for this study. Some physical characteristics (soil porosity and specific gravity) and Total Hydrocarbon Content (THC) of the soil samples were tested for, after the full acclimatization of the soil samples, and at the end of the 10 week experimental period, in accordance with standard methods. Results of the study showed that addition of the compost manure and organic soap the contaminated soil samples significantly (p ≤0.05) degraded the THC, and improved the soil physical characteristics. The result showed that the combination of compost manure and organic soap gave the best remediation result (from 957.21 mg/kg to 154.36 mg/kg), followed by organic soap (from 957.21mg/kg to 203.61 mg/kg), and then compost manure (from 957.21 mg/kg to 262.03 mg/kg). At the end of the experimental period, vegetative growth was observed in the treated soil samples; whereas,  in the control soil samples vegetative growth was absent. Results obtained from this study have shown that amending petroleum products contaminated soils with compost manure and organic soap will enhance remediation of petroleum products contaminated sites.


2016 ◽  
Vol 59 ◽  
pp. 38-47
Author(s):  
Conrad K. Enenebeaku ◽  
Chidozie N. Anyanwu ◽  
Nnaemeka J. Okorocha ◽  
Uchechi E. Enenebeaku ◽  
Emmanuel Nzediegwu ◽  
...  

In order to estimate plant available fraction of metals in two soil samples-contaminated soil (A) and non-contaminated soil (B), a vegetable crop,Curcubita ficifoliawas grown on both soil samples. The matured leaf was harvested and analyzed for its metal concentration after three (3) months of growth. The soil samples were collected before and after planting, digested with acid and analyzed to determine the pseudo total metal concentration and quantification was done using atomic absorption spectroscopy (AAS). To correlate metal accumulation by the vegetable with potential bioavailability of metals in soils, sequential extraction (SE) using the modified BCR technique was performed on the soils. Soil sample B was used for quality control. It was observed that each metal differed considerably in uptake. And theC. ficifoliacultivated on soil sample A had tissue concentrations of Zn, Mn and Cu as follows: 39.6mgkg-1, 18.3mgkg-1and 26.3mgkg-1respectively. Also,C. ficifoliacultivated on soil sample B had a lower absorption of Zn, Mn and Cu with concentrations of 10.21mgkg-1, 9.11mgkg-1, and 7.6mgkg-1respectively. Results of sequential extraction showed that Zn for soil sample A, and Fe for sample B were mostly present in the acid exchangeable and reducible fractions where these metals were mostly taken up.


2011 ◽  
Vol 26 (12) ◽  
pp. 2528 ◽  
Author(s):  
Hideshi Fujiwara ◽  
Katsu Kawabata ◽  
Junji Suzuki ◽  
Osamu Shikino
Keyword(s):  

2009 ◽  
Vol 62-64 ◽  
pp. 451-455 ◽  
Author(s):  
F.A. Aisien ◽  
J.C. Chiadikobi ◽  
E.T. Aisien

This paper considered the toxicity assessment of some crude oil contaminated soils in Niger Delta areas. The soil samples were collected from different horizontal distances, vertical depths and contaminated soil of different ages. The heavy metals in the contaminated soils were digested and extracted using di-acid digested and DTPA extraction methods respectively. The physiochemical parameters (moisture content, pH, N, P and heavy metals (Ni, Pb and Cd) were analysed with APHA method. The heavy metals concentration was determined using atomic absorption spectrophotometer (AAS). The results show that the metals concentration decreased with the age of the contaminated soil and with increased vertical depths. However, the metals concentrations were almost constant at different horizontal distances. Similar trend was observed for the moisture content, pH, N, P and K.


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