Comparative Assessment of Polycyclic Aromatic Hydrocarbon Levels in Indoor and Outdoor Air and Associated Inhalation Health Risks in Akpajo, Alesa and Aleto Communities, Eleme, Rivers State, Nigeria
Jul 2026· Journal of applied chemical science international· Vol 17, pp. 73-87· 0 citations
Abstract
Polycyclic aromatic hydrocarbons (PAHs) are persistent semi-volatile organic contaminants generated mainly during the incomplete combustion of organic materials and petroleum-derived fuels. This study assessed PAH levels in indoor and outdoor air and estimated the associated inhalation health risks in Akpajo, Alesa and Aleto communities of Eleme Local Government Area, Rivers State, Nigeria, an industrially and traffic-influenced area of the Niger Delta. Twelve 24-hour integrated air-sampling conditions were evaluated across three communities, two seasons (dry and wet) and two microenvironments (indoor and outdoor). Airborne particulate-bound PAHs were collected using a high-volume air-sampling approach, solvent-extracted with dichloromethane:n-hexane (1:1, v/v), concentrated and quantified by gas chromatography-mass spectrometry. Method quality control included internal-standard calibration, field and method blanks, duplicate checks, surrogate recovery assessment, blank correction, and limits of detection and quantification. Statistical analysis was based on descriptive statistics, including range, arithmetic mean, pooled congener totals, community means, seasonal means and indoor-outdoor means. Total PAH concentrations ranged from 7.40 µg/m³ in Alesa wet-season indoor air to 30.55 µg/m³ in Aleto dry-season outdoor air. The mean total PAH concentration was highest in Aleto (21.41 µg/m³), followed by Akpajo (11.80 µg/m³) and Alesa (10.39 µg/m³). Dry-season air had a higher mean total PAH concentration (18.18 µg/m³) than wet-season air (10.88 µg/m³), while outdoor air (15.75 µg/m³) exceeded indoor air (13.32 µg/m³). Anthracene, pyrene, benzo(k)fluoranthene, naphthalene, fluorene and phenanthrene were the dominant contributors to the pooled PAH burden. Non-detected high-molecular-weight PAHs were reported as below the method detection limit rather than as true zero values. Screening-level risk assessment showed that children had higher estimated lifetime average daily dose and incremental lifetime carcinogenic risk than adults under the same sampling conditions. The highest child ILCR occurred in Aleto dry-season outdoor air (4.12E-04), while several child-risk estimates exceeded 1.00E-04, indicating potential concern under the assumptions used. The findings indicate measurable PAH contamination, higher dry-season burden and greater screening-level risk estimates for children. Routine monitoring, emission reduction, dust control and targeted public-health communication are recommended.
The results of the total carcinogenic risk for children aged 7–12 years in all schools caused by the presence of PAHs compounds in outdoor environments was acceptable and in some indoor environments, the values at certain schools exceeded the standard threshold of 10− 6-10− 4, indicating potential health risks.
Mohamad Firdaus Ismail, M. F. Fadzil, Nur Atifah binti Mohd Naim et al.· Asian Journal of Atmospheric...· 0 citations
This study evaluated the concentrations of polycyclic aromatic hydrocarbons (PAHs) in soil, water, and edible plants within cashew nut processing clusters in Enugu, Nigeria. Following liquid–liquid and solid–liquid extractions, the concentration of sixteen PAHs congeners were determined using gas chromatography coupled with a flame ionization detector (GC‐FID). To predict the potential sources of these PAHs, a diagnostic ratio guide was employed and principal component analysis was performed. Mutagenic equivalent concentration, human health risk assessment, and ecological risk assessment were performed. The identified PAHs had concentration range: 786.31–2589.46 µg/kg in soil, 33.78–5476.37 µg/L in water, and 561.47–3047.84 µg/kg in vegetables. Except for one location, the vegetables had higher levels of low molecular weight PAHs, while high molecular weight PAHs were more prevalent in the water. The results showed that the studied location has a fair amount of PAH pollution, mostly from pyrogenic sources though the source apportionment models predicted multi‐sources. The ecological risk assessment indicated acenaphthene to be the most contributing contaminant while the health risk evaluations indicated that consumers of water and vegetables from this area may have risk for non‐carcinogenic health problems. There were substantial mutagenic equivalent quantities, and BaP metabolites were probably responsible. The study reveals that inefficient burning of biomass and fossil fuels has resulted in significant levels of PAH contamination in the surrounding cashew nut processing clusters, and these activities should be controlled.
Borehole water is a major drinking water source in Owerri West LGA, Imo State, Nigeria, but fuel
stations within residential areas raise concerns over groundwater contamination by polycyclic
aromatic hydrocarbons (PAHs). This study assessed concentrations of the 16 USEPA priority
PAHs in borehole water near three fuel stations (Nekede, Orogwe, Obinze), evaluated health risks
to adults and children, and identified probable contamination sources. Twenty-seven samples were
collected in the dry season from fuel-station and nearby residential boreholes (25–625 m away).
Physicochemical parameters were analyzed per APHA (2017); PAHs were extracted (USEPA
Method 3510C) and quantified by GC-MS. Health risk was assessed using the USEPA (2014)
deterministic model, with source apportionment via diagnostic ratios and PCA. All
physicochemical parameters met WHO/USEPA limits. Total PAHs (Σ16PAHs) ranged from
0.112–0.217 mg/L, with benzo(a)pyrene exceeding the USEPA limit (0.01 µg/L) in all fuel-station
boreholes. Hazard quotients were below 1, but benzo(a)pyrene cancer risk (7.15×10⁻⁵ adults;
1.67×10⁻⁴ children, Nekede) exceeded the USEPA threshold (1×10⁻⁶), with children ~2.3 times
more at risk. Diagnostic ratios indicated predominantly pyrogenic sources with petrogenic
contribution from fuel leaks. Despite meeting potability standards, the water posed unacceptable
carcinogenic risk, warranting setback regulations and household treatment.
Dike Chinyere L., Oze R. N., Bilar A. et al.· INTERNATIONAL JOURNAL OF CHE...· 0 citations
Background: Oil spillage is a major driver of soil degradation in the Niger Delta, yet integrated, site-specific assessments coupling metals, polycyclic aromatic hydrocarbons (PAHs) and quantitative risk remain scarce.
Objective: This study assessed the contamination status, source structure and ecological and human-health risk of soils at a crude-oil spill site in Okpohovor, Udu Local Government Area, Delta State, Nigeria.
Methods: Soils from five points (S1–S5) and a control station were sampled at two depths (0–15 and 15–30 cm). pH, electrical conductivity, total organic carbon, particle size and nine metals were determined by flame atomic absorption spectrophotometry, and 16 priority PAHs by GC–MS. Pollution indices, principal component analysis (PCA), one-way ANOVA with effect sizes, and BaP-equivalent, hazard-index and incremental lifetime cancer-risk models were applied.
Results: Soils were strongly acidic (pH 3.00–3.70) and sandy. All metals were below Department of Petroleum Resources (DPR) target values except cadmium (0.05–2.55 mg/kg), which reached the pollution range in 60% of samples. Clay differed significantly between sites (F=10.133, p=0.013, η²=0.890). PCA separated a lithogenic Pb–Cr–Ni–Fe association (PC1, 32.0%) from a cadmium-driven signal. The ecological risk index (9–263) was cadmium-dominated. ΣPAH reached 81,327 µg/kg from mixed petrogenic–pyrogenic sources; hazard indices were mostly below 1 but total cancer risk exceeded 1×10⁻⁶.
Conclusion: Cadmium and carcinogenic PAHs are the priority contaminants, posing food-chain and public-health risks that warrant targeted remediation and sustained monitoring.
Peter Mamuro Eguvbe, Solomon Erhajemu Ogoron, E. W. Odali et al.· Sriwijaya Journal of Environ...· 0 citations
Persistent and semi-volatile organic contaminants remain important atmospheric tracers because of their environmental persistence, multiple emission pathways and capacity for regional transport. This study investigated the spatial and seasonal variability of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in northeastern France. Nitrogen-doped carbon-coated silicon carbide foam (NMC@SiC) passive air samplers were deployed at six urban, suburban and rural sites in the Strasbourg metropolitan area between 2018 and 2020. Twenty-one OCPs, sixteen PAHs, and twenty-two PCBs were quantified by gas chromatography-tandem mass spectrometry. PAHs exhibited the clearest spatial and seasonal variability, with higher concentrations at urban sites and cold-season or autumn enhancements depending on the location. Naphthalene dominated the PAH profile, while diagnostic ratios suggested dominant combustion inputs, including traffic, residential heating and biomass or solid-fuel burning. PCBs showed weaker spatial contrasts and more homogeneous distributions, with profiles dominated by penta-, hexa- and hepta-chlorinated congeners, indicating diffuse legacy contamination, possible PCB-containing materials, industrially influenced areas and regional redistribution. OCPs were dominated by dichlorodiphenyltrichloroethane-related compounds and hexachlorocyclohexane isomers, reflecting historical residues and secondary volatilization from contaminated environmental reservoirs. These findings highlight the combined influence of current urban emissions, persistent legacy reservoirs, secondary re-emissions and regional atmospheric transport on organic contaminant distributions in northeastern France.
Dani Khoury, Supansa Chimjarn, O. Delhomme et al.· Environment International· 0 citations