Analytical Concordance of EDTA Complexometry and Atomic Absorption Spectrometry in Assessing Alkaline Earth Metal Profiles of Commercial Table Water Sold in Okigwe Town
Eberendu, Kizito O.1*, Nlemchukwu Benedict N.C.1, Ejezie, Michael U.1,
Ukachukwu Veronica I.1, Eberendu Stella U.2, Emele Hyacinth C.1
1Department of Chemistry, University of Agriculture and Environmental Sciences, Umuagwo, Nigeria.
2Department of Mass Communication, Abia State University, Uturu, Nigeria.
*Corresponding Author E-mail: kizito.onyedikachi@uaes.edu.ng
ABSTRACT:
Both economical progress and human health depend on having access to clean, safe drinking water1. In many regions, including Nigeria, packaged drinking water has become a major source of potable water due to inadequate municipal water supply systems. The quality of packaged drinking water is therefore of significant public health concern.
Calcium and magnesium are naturally occuring alkaline earth metals commonly found in groundwater and surface water sources. These metals are the principal contributors to water hardness and play vital roles in human physiology, including bone mineralization, enzymatic activity, cardiovascular regulation, and neuromuscular function6,7. Epidemiological studies have shown that moderate intake of calcium and magnesium through drinking water is associated with beneficial health outcomes, particularly reduced risks of cardiovascular diseases, whereas extremely low or excessive concentrations may lead to adverse health effects8,9.
Analytical determination of calcium and magnesium in water is essential for quality assessment and regulatory compliance. Complexometric titration using ethylenediaaminetetraacetic acid (EDTA) is a classical analytical technique widely employed due to its simplicity and cost-effectiveness3,10. However, this method is susceptible to endpoint detection errors. Atomic absorption spectrophotometry (AAS) is an instrumental technique known for its high sensitivity, selectivity, and precision in metal analysis4,11,12.
Comparative evaluation of classical and instrumental analytical methods is important for selecting appropriate techniques for routine water quality monitoring. This study therefore aims to determine calcium and magnesium concentrations in packaged drinking water sold in Okigwe Town using EDTA titration and AAS, and to compare the analytical performance of both methods with reference to international drinking water standards.
MATERIALS AND METHODS:
Sample Collection:
Commercially packaged drinking water samples were randomly purchased from retail outlets within Okigwe Town, Imo State, Nigeria. To avoid contamination, all samples were brought to the lab in their original, sealed containers and kept at room temperature until analysis.
Reagents and Apparatus:
All reagents used were of analytical grade. Standard solutions of EDTA, calcium, and magnesium were prepared using distilled water. Apparatus used included burettes, pipettes, volumetric flasks, conical flasks, a pH meter, and an atomic absorption spectrophotometer equipped with calcium and magnesium hollow cathode lamps.
Standard complexometric titration techniques were used to measure the amounts of calcium and magnesium. The water samples were buffered to the required pH and titrated against standardized EDTA solution using appropriate indicators. The endpoint was identified by a distinct colour change, and concentrations were calculated from the volume of EDTA consumed.
Atomic absorption spectrophotometric analysis was carried out after calibrating the instrument with standard solutions of calcium and magnesium. Absorbance measurements were taken at the distinctive wavelengths for each metal after samples were sucked straight into the flames. Concentrations were obtained from calibration curves.
Results obtained from both analytical methods were compared, and measured concentrations were evaluated against World Health Organization drinking water standards.
Results:
The concentrations of calcium and magnesium in the packaged drinking water samples were successfully determined using both EDTA complexometric titration and atomic absorption spectrophotometry (Tables 1 and 2).
Calcium concentrations varied among the sampled water brands. EDTA titration produced consistent values across samples, while AAS generally yielded slightly higher concentrations, indicating greater sensitivity. All calcium concentrations obtained were within WHO permissible limits for drinking water.
Magnesium concentrations also showed variations among the samples. Results obtained using EDTA titration were reproducible; however, AAS analysis provided more precise measurements, particularly for samples with lower magnesium content. All magnesium concentrations were within WHO recommended limits.
Table 1: Calcium and Magnesium of water determined by AAS analysis (mg/L)
|
Element |
Water sample (mg/L) |
||||||||||
|
BLANK |
COF |
BEN |
MAK |
IVO |
MAT |
JON |
ALK |
DOO |
SMAR |
NIC |
|
|
Sample No.: |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
|
Calcium |
0.90 |
2.80 |
2.05 |
2.14 |
2.44 |
0.98 |
1.44 |
2.22 |
3.00 |
2.40 |
1.10 |
|
Magnesium |
0.75 |
0.98 |
1.54 |
1.11 |
1.15 |
1.00 |
1.19 |
0.99 |
1.14 |
1.20 |
1.35 |
Table 2: Calcium and Magnesium of water determined by Complexometric Method (mg/L)
|
Element |
Water sample (mg/L) |
||||||||||
|
BLANK |
COF |
BEN |
MAK |
IVO |
MAT |
JON |
ALK |
DOO |
SMAR |
NIC |
|
|
Sample No.: |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
|
Calcium |
1.85 |
3.31 |
3.35 |
3.62 |
2.95 |
2.76 |
2.62 |
3.00 |
2.82 |
3.12 |
3.11 |
|
Magnesium |
1.00 |
2.80 |
1.68 |
2.13 |
2.11 |
2.30 |
1.65 |
1.73 |
1.62 |
1.78 |
1.20 |
* COFO = COF, BENOBLE = BEN, MAKAGINUS = MAK, IVON = IVO, MATRIX = MAT, JONUK = JON, ALKALINE = ALK, DOOM = DOO, SMART ICE = SMA, and DE NICE = NIC
Overall, both methods exhibited similar trends in calcium and magnesium distribution across the samples, with AAS demonstrating superior analytical performance.
The variations in calcium and magnesium concentrations observed among the packaged drinking water samples may be attributed to differences in water sources, geological formations, and treatment processes employed by manufacturers5,12. The presence of these minerals confirms their natural occurrence in drinking water and their contribution to water hardness.
The EDTA titration method proved suitable for routine analysis due to its simplicity and affordability, consistent with previous studies2,13,14. However, the reliance on visual endpoint detection may introduce minor errors. Atomic absorption spectrophotometry minimized subjective errors and provided improved sensitivity and precision, particularly for low-level metal determination4.
The findings of this study are in agreement with earlier reports highlighting the advantages of instrumental methods over classical titrimetric techniques for trace metal analysis in water5,15. Nevertheless, both methods were adequate for assessing compliance with drinking water quality standards.
This study demonstrates that both EDTA complexmetric titration and atomic absorption spectrophotometry are effective for the determination of calcium and magnesium in packaged drinking water. While EDTA titration is cost-effective and suitable for routine monitoring, atomic absorption spectrophotometry offers superior sensitivity and precision. All water samples analyzed complied with World Health Organization standards for calcium and magnesium, indicating that they are safe for human consumption with respect to these parameters.
The authors acknowledge the Department of Chemistry laboratories for providing the facilities and technical assistance required for this research.
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Received on 02.02.2026 Revised on 13.04.2026 Accepted on 15.05.2026 Published on 04.07.2026 Available online from July 30, 2026 Asian J. Research Chem.2026; 19(4):287-289. DOI: 10.52711/0974-4150.2026.00044 ©A and V Publications All Right Reserved
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