Pub Date : 2026-02-01Epub Date: 2026-01-24DOI: 10.1016/j.hazadv.2026.101035
Eva Martinková, Ondřej Šebek, Alexandre V. Andronikov, Markéta Štěpánová, Jan Čuřík, František Veselovský, Zuzana Čvančarová, Anna Vynnychuk, Tamara Sidorinová
This study evaluates the influence of digestion methods on metal concentrations and results of isotopic analysis of dusts generated during electronic waste processing. E-waste dusts were collected from processing units such as photovoltaic panels, LCD and CRT monitors, and mixed e-waste. Following methods were used for digestion: i) aqua regia with a temperature pretreatment at 110°C, ii) concentrated acids (HClO4, HF, HNO3) with a temperature pretreatment at 550°C. Results showed that concentrated acids with 550°C pretreatment generally yielded significantly higher recoveries for most elements (e.g., Ag, Al, Ba, K, Na, Pb). Conversely, aqua regia was more efficient for Sn recovery, as the higher temperature used with concentrated acids led to the formation of volatile SnCl₄ and subsequent Sn loss. A significant Pb isotopic shift was observed between the two methods in glass-rich samples, indicating that aqua regia leached readily available Pb, while concentrated acids (mostly HF) released Pb (of different origin) incorporated within the glass. The isotopic analyses revealed consistent δ66/64Zn (-0.078 to 0.052) and δ65/63Cu values (0.170 to 0.313) across both methods. Slight changes in δ66/64Zn and δ114/110Cd values were attributed to sample heterogeneity, origin or phase changes after higher temperature treatment at 550°C. A distinct Cu isotopic signature (δ65/63Cu 0.067 and 0.078) in CRT dust suggests a different historical origin of Cu in older devices. These findings highlight the crucial role of selecting a digestion method that is appropriate for the specific e-waste dust, to ensure accurate elemental and isotopic analysis.
{"title":"Effect of digestion method on elemental concentrations and Cd, Cu, Zn and Pb isotopic signatures of e‑waste dust from different processing units","authors":"Eva Martinková, Ondřej Šebek, Alexandre V. Andronikov, Markéta Štěpánová, Jan Čuřík, František Veselovský, Zuzana Čvančarová, Anna Vynnychuk, Tamara Sidorinová","doi":"10.1016/j.hazadv.2026.101035","DOIUrl":"10.1016/j.hazadv.2026.101035","url":null,"abstract":"<div><div>This study evaluates the influence of digestion methods on metal concentrations and results of isotopic analysis of dusts generated during electronic waste processing. E-waste dusts were collected from processing units such as photovoltaic panels, LCD and CRT monitors, and mixed e-waste. Following methods were used for digestion: i) aqua regia with a temperature pretreatment at 110°C, ii) concentrated acids (HClO<sub>4</sub>, HF, HNO<sub>3</sub>) with a temperature pretreatment at 550°C. Results showed that concentrated acids with 550°C pretreatment generally yielded significantly higher recoveries for most elements (e.g., Ag, Al, Ba, K, Na, Pb). Conversely, aqua regia was more efficient for Sn recovery, as the higher temperature used with concentrated acids led to the formation of volatile SnCl₄ and subsequent Sn loss. A significant Pb isotopic shift was observed between the two methods in glass-rich samples, indicating that aqua regia leached readily available Pb, while concentrated acids (mostly HF) released Pb (of different origin) incorporated within the glass. The isotopic analyses revealed consistent δ<sup>66/64</sup>Zn (-0.078 to 0.052) and δ<sup>65/63</sup>Cu values (0.170 to 0.313) across both methods. Slight changes in δ<sup>66/64</sup>Zn and δ<sup>114/110</sup>Cd values were attributed to sample heterogeneity, origin or phase changes after higher temperature treatment at 550°C. A distinct Cu isotopic signature (δ<sup>65/63</sup>Cu 0.067 and 0.078) in CRT dust suggests a different historical origin of Cu in older devices. These findings highlight the crucial role of selecting a digestion method that is appropriate for the specific e-waste dust, to ensure accurate elemental and isotopic analysis.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 101035"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146077263","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-13DOI: 10.1016/j.hazadv.2025.100977
S. Trotta , G. Binda , M.F. Ferrario , A. Pozzi , A.M. Michetti
The mobility of arsenic (As) in groundwater is governed by dynamic interactions at the sediment-water interface, where both mineral reactivity and aqueous chemistry play key roles. In the Como aquifer (Northern Italy), As distribution is vertically heterogeneous: shallow horizons remain below the WHO limit of 10 µg/L, whereas deeper zones reach concentrations up to 250 µg/L. Although this variability is well documented, the underlying mechanisms remain only partially understood. To address this gap, we performed batch experiments on shallow and deep aquifer sediments with contrasting composition, systematically varying pH, electrical conductivity, and dissolved organic carbon in a full-factorial design of experiment. Results revealed nonlinear adsorption responses and sediment-specific behaviours. Shallow sediments exhibited stronger and more stable As retention, associated with higher contents of Fe-, Al-, and Mn-(hydr)oxides and greater cation exchange capacity. In contrast, deep-aquifer sediments showed weaker and more variable adsorption, especially under acidic, DOC-enriched, and high-conductivity conditions. Response surface models confirmed that sediment composition governs As retention capacity, while water chemistry modulates its efficiency. This integrative approach links laboratory adsorption patterns with field-scale As distribution, providing a mechanistic explanation for the observed vertical heterogeneity in the Como aquifer and supporting predictive assessment of groundwater vulnerability.
{"title":"A design of experiments approach to arsenic retention: Interactions between sediment properties and water chemistry","authors":"S. Trotta , G. Binda , M.F. Ferrario , A. Pozzi , A.M. Michetti","doi":"10.1016/j.hazadv.2025.100977","DOIUrl":"10.1016/j.hazadv.2025.100977","url":null,"abstract":"<div><div>The mobility of arsenic (As) in groundwater is governed by dynamic interactions at the sediment-water interface, where both mineral reactivity and aqueous chemistry play key roles. In the Como aquifer (Northern Italy), As distribution is vertically heterogeneous: shallow horizons remain below the WHO limit of 10 µg/L, whereas deeper zones reach concentrations up to 250 µg/L. Although this variability is well documented, the underlying mechanisms remain only partially understood. To address this gap, we performed batch experiments on shallow and deep aquifer sediments with contrasting composition, systematically varying pH, electrical conductivity, and dissolved organic carbon in a full-factorial design of experiment. Results revealed nonlinear adsorption responses and sediment-specific behaviours. Shallow sediments exhibited stronger and more stable As retention, associated with higher contents of Fe-, Al-, and Mn-(hydr)oxides and greater cation exchange capacity. In contrast, deep-aquifer sediments showed weaker and more variable adsorption, especially under acidic, DOC-enriched, and high-conductivity conditions. Response surface models confirmed that sediment composition governs As retention capacity, while water chemistry modulates its efficiency. This integrative approach links laboratory adsorption patterns with field-scale As distribution, providing a mechanistic explanation for the observed vertical heterogeneity in the Como aquifer and supporting predictive assessment of groundwater vulnerability.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100977"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145790578","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Springs are a major supply of drinking water for many rural communities, but both geogenic and human activities are posing an increasing threat to their quality. Despite their significance, spring systems in study area are not well researched and no prior study has provided a thorough examination combining physicochemical profiling, heavy metal estimation and microbiological examination. In this study, thirty-six spring water samples from various regions across Azad Jammu and Kashmir (AJK) were examined to determine their potability and chemical composition. Physicochemical analysis, heavy metal quantification, and microbiological evaluation followed by Statistical analyses, such as Principal Component Analysis (PCA) and Pearson correlation, were performed to recognize key patterns and source contamination. Over 80% of the samples were classified as "unsuitable for drinking," based on WHO standards, according to the Water Quality Index values ranging from 397.6 to 2008.2. In most of the samples elevated toxic heavy metal levels, including nickel (0.09-0.25 mg/L), lead (0.49-2.21 mg/L), and cadmium (0.03-0.06 mg/L), were observed. Microbiological contamination was also common; in most springs, levels of E. coli, fecal coliforms, and total coliforms were found to be within dangerous ranges. With considerable loadings from bacteria, chemical oxygen demand, and nutritional factors, Principal Component Analysis (PCA) revealed two main components that account for more than 60% of the variance. The hydro chemical facies obtained from the Piper diagram showed that Ca–Mg–SO4 type water predominated. This study provides first-region specific baseline data set employing an integrated analytical approach, offering new insights into the spring profile of the area. Results obtained highlight urgent need to conduct routine monitoring, raise community awareness, and implement legislative changes to protect spring water sources. The findings of the study offer vital comprehension for water resource planners, environmental managers, and local health authorities looking to enhance water quality and protect public health in the area.
{"title":"Unveiling water quality patterns in the non-industrial mountainous region of northern Pakistan: A hydrological perspective","authors":"Eena Sadaf , Rashid Khan , Amina Azhar , Muhammad Faraz Bhatti , Saadia Andleeb , Sughra Sarwar , Muhammad Kamran Khan","doi":"10.1016/j.hazadv.2025.100987","DOIUrl":"10.1016/j.hazadv.2025.100987","url":null,"abstract":"<div><div>Springs are a major supply of drinking water for many rural communities, but both geogenic and human activities are posing an increasing threat to their quality. Despite their significance, spring systems in study area are not well researched and no prior study has provided a thorough examination combining physicochemical profiling, heavy metal estimation and microbiological examination. In this study, thirty-six spring water samples from various regions across Azad Jammu and Kashmir (AJK) were examined to determine their potability and chemical composition. Physicochemical analysis, heavy metal quantification, and microbiological evaluation followed by Statistical analyses, such as Principal Component Analysis (PCA) and Pearson correlation, were performed to recognize key patterns and source contamination. Over 80% of the samples were classified as \"unsuitable for drinking,\" based on WHO standards, according to the Water Quality Index values ranging from 397.6 to 2008.2. In most of the samples elevated toxic heavy metal levels, including nickel (0.09-0.25 mg/L), lead (0.49-2.21 mg/L), and cadmium (0.03-0.06 mg/L), were observed. Microbiological contamination was also common; in most springs, levels of <em>E. coli</em>, fecal coliforms, and total coliforms were found to be within dangerous ranges. With considerable loadings from bacteria, chemical oxygen demand, and nutritional factors, Principal Component Analysis (PCA) revealed two main components that account for more than 60% of the variance. The hydro chemical facies obtained from the Piper diagram showed that Ca–Mg–SO<sub>4</sub> type water predominated. This study provides first-region specific baseline data set employing an integrated analytical approach, offering new insights into the spring profile of the area. Results obtained highlight urgent need to conduct routine monitoring, raise community awareness, and implement legislative changes to protect spring water sources. The findings of the study offer vital comprehension for water resource planners, environmental managers, and local health authorities looking to enhance water quality and protect public health in the area.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100987"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924650","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In this study, the contributions of wastewater treatment plants (WWTPs) to emerging contaminants in the environment were monitored. Samples were collected at nine WWTPs with sampling on three separate days at each WWTP. The WWTPs used the different secondary treatment methods as follows: conventional activated sludge (WWTPs 1, 2, and 9), aerobic contact oxidation (WWTPs 5 and 6), and oxidation ditch (WWTPs 3, 4, 7 and 8). A significant matrix effect was observed in primary effluent samples but not in secondary and final effluent samples. The matrix effect was more pronounced during sample preparation using solid-phase extraction. Triethylene glycol dimethyl ether and glycidyl methacrylate had high removal rates (> 50 %) with all three treatment methods. By contrast, tebuconazole and bromobutide had low removal rates or were not removed by any of the treatment methods. Thirteen compounds in various chemical classes were prioritized on the basis of their concentrations in the final effluent relative to their predicted no-effect concentrations. These compounds were surfactants (diethanolamine and N-methyldidecylamine), an industrial solvent (dicyclohexylamine), herbicides (2,4-dicholorophenoxyacetic acid, bromobutide, and butachlor/pretilachlor), an antiseptic (triclosan [and its chlorinated adducts]), industrial chemicals (hexamethylene diacrylate, pyridine, and decanoic acid), plasticizers (tributyl phosphate and tricresyl phosphate), and a corrosion inhibitor (N,N-dimethyldodecylamine). Our results imply that WWTPs are sources of these compounds in the environment. These compounds could threaten ecosystems in receiving waterbodies and future studies should monitor release of these emerging contaminants from WWTPs.
{"title":"Priority list of emerging contaminants in domestic wastewater treatment plants and their removal by different secondary treatment methods","authors":"Aishwarya Pandey , Ikuro Kasuga , Hiroaki Furumai , Futoshi Kurisu","doi":"10.1016/j.hazadv.2025.100969","DOIUrl":"10.1016/j.hazadv.2025.100969","url":null,"abstract":"<div><div>In this study, the contributions of wastewater treatment plants (WWTPs) to emerging contaminants in the environment were monitored. Samples were collected at nine WWTPs with sampling on three separate days at each WWTP. The WWTPs used the different secondary treatment methods as follows: conventional activated sludge (WWTPs 1, 2, and 9), aerobic contact oxidation (WWTPs 5 and 6), and oxidation ditch (WWTPs 3, 4, 7 and 8). A significant matrix effect was observed in primary effluent samples but not in secondary and final effluent samples. The matrix effect was more pronounced during sample preparation using solid-phase extraction. Triethylene glycol dimethyl ether and glycidyl methacrylate had high removal rates (> 50 %) with all three treatment methods. By contrast, tebuconazole and bromobutide had low removal rates or were not removed by any of the treatment methods. Thirteen compounds in various chemical classes were prioritized on the basis of their concentrations in the final effluent relative to their predicted no-effect concentrations. These compounds were surfactants (diethanolamine and <em>N</em>-methyldidecylamine), an industrial solvent (dicyclohexylamine), herbicides (2,4-dicholorophenoxyacetic acid, bromobutide, and butachlor/pretilachlor), an antiseptic (triclosan [and its chlorinated adducts]), industrial chemicals (hexamethylene diacrylate, pyridine, and decanoic acid), plasticizers (tributyl phosphate and tricresyl phosphate), and a corrosion inhibitor (<em>N,N</em>-dimethyldodecylamine). Our results imply that WWTPs are sources of these compounds in the environment. These compounds could threaten ecosystems in receiving waterbodies and future studies should monitor release of these emerging contaminants from WWTPs.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100969"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924731","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-09DOI: 10.1016/j.hazadv.2025.100967
Mark E. Fuller , Paul C. Hedman , Nikita Thakur , Danielle N. Tran , Charles E. Schaefer
Stockpiles of aging, off-spec, or other military munitions containing energetic formulations pose a health and safety risk to humans and the environment. This research is the first report demonstrating electrochemical demilitarization of solid Composition B (CompB; HMX/RDX/TNT) and nitrocellulose (NC) fines. The process combined alkaline hydrolysis with cathode surface reactions in a divided electrochemical cell configuration. The constituents of CompB were degraded (>95 %) to simple end products consisting primarily of NO2−, formaldehyde, and residual color. The latter two compounds were shown to be readily amenable to an UV/H2O2 treatment as a potential polishing step. NC fines were hydrolyzed to NO2−, NO3−, NH4+ and unspecified total organic carbon (TOC) and total Kjeldahl nitrogen (TKN), with minimal accumulation of free cyanide. For both energetics, the degradation kinetics were improved by heating the system to 50 °C. The estimated cost of treatment at the elevated temperature, including chemicals and energy, was <$0.05 per g for CompB and between $0.18 and $0.29 per g for NC, depending on the size cutoff for residuals (>5 and >1.5 µm, respectively). These results provide proof-of-concept that electrochemical processes for treating solid energetic materials may be an effective approach for safe and efficient demilitarization treatment trains for military munitions.
{"title":"Electrochemical demilitarization of solid composition B (HMX/RDX/TNT) and nitrocellulose","authors":"Mark E. Fuller , Paul C. Hedman , Nikita Thakur , Danielle N. Tran , Charles E. Schaefer","doi":"10.1016/j.hazadv.2025.100967","DOIUrl":"10.1016/j.hazadv.2025.100967","url":null,"abstract":"<div><div>Stockpiles of aging, off-spec, or other military munitions containing energetic formulations pose a health and safety risk to humans and the environment. This research is the first report demonstrating electrochemical demilitarization of solid Composition B (CompB; HMX/RDX/TNT) and nitrocellulose (NC) fines. The process combined alkaline hydrolysis with cathode surface reactions in a divided electrochemical cell configuration. The constituents of CompB were degraded (>95 %) to simple end products consisting primarily of NO<sub>2</sub><sup>−</sup>, formaldehyde, and residual color. The latter two compounds were shown to be readily amenable to an UV/H<sub>2</sub>O<sub>2</sub> treatment as a potential polishing step. NC fines were hydrolyzed to NO<sub>2</sub><sup>−</sup>, NO<sub>3</sub><sup>−</sup>, NH<sub>4</sub><sup>+</sup> and unspecified total organic carbon (TOC) and total Kjeldahl nitrogen (TKN), with minimal accumulation of free cyanide. For both energetics, the degradation kinetics were improved by heating the system to 50 °C. The estimated cost of treatment at the elevated temperature, including chemicals and energy, was <$0.05 per g for CompB and between $0.18 and $0.29 per g for NC, depending on the size cutoff for residuals (>5 and >1.5 µm, respectively). These results provide proof-of-concept that electrochemical processes for treating solid energetic materials may be an effective approach for safe and efficient demilitarization treatment trains for military munitions.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100967"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924735","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Polystyrene nanoplastics (PS-NPs) are emerging environmental contaminants that can cross biological barriers and accumulate in the reproductive organs. This study evaluated developmental ovarian toxicity after maternal and lactational PS-NP exposure in rats on gestational day 20 (GD20) and postnatal days 30 and 60 (PD30, PD60). Pregnant Sprague–Dawley rats were administered PS-NPs at doses of 0.1, 1, or 10 mg/kg/day during gestation and lactation. At GD20, fetal ovaries from exposed dams showed a significant reduction in primordial follicle number and diameter, early granulosa cell disorganization, and a lower parenchyma-to-stroma ratio, indicating impaired folliculogenesis. By PD30 and PD60, ovarian alterations intensified in a dose-dependent manner, including granulosa layer thinning, follicular degeneration, and cortical disarray, which were most pronounced in the high-dose group. Fluorescence microscopy confirmed the transplacental and lactational transfer of rhodamine-labeled PS-NPs, with persistent and dose-dependent accumulation in the follicles and stroma. Biochemically, PS-NP exposure increased the total oxidant status (TOS) and oxidative stress index (OSI) while decreasing the total antioxidant capacity (TAC). Serum estradiol and progesterone levels declined markedly, consistent with oxidative and endocrine disruption. Immunohistochemistry revealed the upregulation of P53 and downregulation of BCL-2, indicating apoptosis-mediated ovarian injury. These findings demonstrate that combined gestational and lactational PS-NP exposure causes persistent, dose-dependent ovarian damage from the fetal stage through postnatal development, highlighting the reproductive risks associated with maternal nanoplastic exposure in an increasingly polluted environment.
{"title":"Transplacental and lactational transfer of polystyrene nanoplastics leads to long-term ovarian impairment in rat offspring","authors":"Mohammad Bostanifard , Hamid Reza Moradi , Zabihollah Khaksar , Sajjad Abbasi , Behzad Shirkavand Hadavand , Milad Faraji","doi":"10.1016/j.hazadv.2026.101007","DOIUrl":"10.1016/j.hazadv.2026.101007","url":null,"abstract":"<div><div>Polystyrene nanoplastics (PS-NPs) are emerging environmental contaminants that can cross biological barriers and accumulate in the reproductive organs. This study evaluated developmental ovarian toxicity after maternal and lactational PS-NP exposure in rats on gestational day 20 (GD20) and postnatal days 30 and 60 (PD30, PD60). Pregnant Sprague–Dawley rats were administered PS-NPs at doses of 0.1, 1, or 10 mg/kg/day during gestation and lactation. At GD20, fetal ovaries from exposed dams showed a significant reduction in primordial follicle number and diameter, early granulosa cell disorganization, and a lower parenchyma-to-stroma ratio, indicating impaired folliculogenesis. By PD30 and PD60, ovarian alterations intensified in a dose-dependent manner, including granulosa layer thinning, follicular degeneration, and cortical disarray, which were most pronounced in the high-dose group. Fluorescence microscopy confirmed the transplacental and lactational transfer of rhodamine-labeled PS-NPs, with persistent and dose-dependent accumulation in the follicles and stroma. Biochemically, PS-NP exposure increased the total oxidant status (TOS) and oxidative stress index (OSI) while decreasing the total antioxidant capacity (TAC). Serum estradiol and progesterone levels declined markedly, consistent with oxidative and endocrine disruption. Immunohistochemistry revealed the upregulation of P53 and downregulation of BCL-2, indicating apoptosis-mediated ovarian injury. These findings demonstrate that combined gestational and lactational PS-NP exposure causes persistent, dose-dependent ovarian damage from the fetal stage through postnatal development, highlighting the reproductive risks associated with maternal nanoplastic exposure in an increasingly polluted environment.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 101007"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924806","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-11-20DOI: 10.1016/j.hazadv.2025.100944
Lin Sun , Wenge Zhang , Wenyu Bai , Hao Gan , Bo Xu , Jing Wang , Yanhui Liu , Chunmei Geng , Wen Yang
Volatile Organic Compounds (VOCs) are priority tropospheric pollutants, characterized by high chemical reactivity and adverse health effects. Industrial emission is a major VOC source, yet studies on its characteristics in industrial parks within Zibo remain limited. This research investigates VOC emissions at two sites (X1 and X2) within an industrial park in Zibo during the summer of 2021, focusing on their sources, chemical impacts, and health risks. Mobile, petrochemical industry and solvent usage were identified as the predominant anthropogenic contributors at both sites. Alkene (X1: 54.71 ppbv, X2: 48.94 ppbv) was the key ozone precursor, and petrochemical industry was the largest contributor to ozone formation (X1: 33.83 ppbv, X2: 40.10 ppbv). As a typical tracer of biogenic emissions and a key contributor to ozone formation, our identification of significant industrial isoprene emissions suggests the potential for its anthropogenic regulation. Health risk assessment revealed acrolein and 1,3-butadiene as the dominant contributors to non-carcinogenic risk (expressed by hazard ratio, X1: 8.62, X2: 4.19) and carcinogenic risk (expressed by lifetime cancer risk, X1: 2.12×10−5, X2: 2.38×10−5), respectively. Solvent usage (hazard ratio: 4.76, lifetime cancer risk:1.70×10−5) contributed most at X1, while petrochemical industry (hazard ratio: 2.45, lifetime cancer risk:3.35×10−5) was the largest contributor at X2. These findings underscore the need for source-specific mitigation strategies to effectively mitigate ozone and alleviate health risks in industrial regions.
{"title":"Source appointment, chemical impacts and health risk of volatile organic compounds in an industrial park in Zibo, China","authors":"Lin Sun , Wenge Zhang , Wenyu Bai , Hao Gan , Bo Xu , Jing Wang , Yanhui Liu , Chunmei Geng , Wen Yang","doi":"10.1016/j.hazadv.2025.100944","DOIUrl":"10.1016/j.hazadv.2025.100944","url":null,"abstract":"<div><div>Volatile Organic Compounds (VOCs) are priority tropospheric pollutants, characterized by high chemical reactivity and adverse health effects. Industrial emission is a major VOC source, yet studies on its characteristics in industrial parks within Zibo remain limited. This research investigates VOC emissions at two sites (X1 and X2) within an industrial park in Zibo during the summer of 2021, focusing on their sources, chemical impacts, and health risks. Mobile, petrochemical industry and solvent usage were identified as the predominant anthropogenic contributors at both sites. Alkene (X1: 54.71 ppbv, X2: 48.94 ppbv) was the key ozone precursor, and petrochemical industry was the largest contributor to ozone formation (X1: 33.83 ppbv, X2: 40.10 ppbv). As a typical tracer of biogenic emissions and a key contributor to ozone formation, our identification of significant industrial isoprene emissions suggests the potential for its anthropogenic regulation. Health risk assessment revealed acrolein and 1,3-butadiene as the dominant contributors to non-carcinogenic risk (expressed by hazard ratio, X1: 8.62, X2: 4.19) and carcinogenic risk (expressed by lifetime cancer risk, X1: 2.12×10<sup>−5</sup>, X2: 2.38×10<sup>−5</sup>), respectively. Solvent usage (hazard ratio: 4.76, lifetime cancer risk:1.70×10<sup>−5</sup>) contributed most at X1, while petrochemical industry (hazard ratio: 2.45, lifetime cancer risk:3.35×10<sup>−5</sup>) was the largest contributor at X2. These findings underscore the need for source-specific mitigation strategies to effectively mitigate ozone and alleviate health risks in industrial regions.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100944"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-11-30DOI: 10.1016/j.hazadv.2025.100959
Xinjie Xiao , Wei Wu , Juanjuan Zhang , Qijiong Zhu , Yilin Li , Yayi Li , Haoyi Feng , Wan Peng , Jianxiong Hu , Dan Cai , Hongwei Tu , Guanhao He , Wenjun Ma , Tao Liu
Against the backdrop of global aging, rising risks of chronic diseases and multimorbidity pose considerable public health challenges. To investigate the association of long-term exposure to fine particulate matter (PM2.5) and its chemical components with multimorbidity development, this prospective cohort study included 8,257 participants from the China Health and Retirement Longitudinal Study (CHARLS) cohort (2011–2020). PM2.5 mass and its chemical components (sulfate [SO42-], nitrate [NO3-], ammonium [NH4+], organic matter [OM], and black carbon [BC]) were evaluated by city-level three-year average exposures. Multistate models were used to estimate the hazard ratios (HRs) for chronic disease accumulation and death, and the corresponding population-attributable fractions (PAFs) attributable to PM2.5 mass and its chemical components were also calculated. For single chronic disease patients, each standard deviation (SD = 14.2 μg/m³) increase in PM2.5 mass concentration was associated with HRs of 1.46 and 2.14 for basic multimorbidity and death, respectively. Among those with basic multimorbidity, each SD increase yielded HRs of 1.31 for complex multimorbidity and 2.20 for death. BC showed the strongest association with multimorbidity development, followed by SO42-, OM, NH4+, and NO3-. Achieving China's Grade II PM2.5 standard (35 μg/m³) could avert 19.32% of transitions from one disease to basic multimorbidity and 13.86% of transitions from basic to complex multimorbidity. Long-term exposure to PM2.5 mass and its chemical components was associated with increased risks across all disease stages of multimorbidity development. Targeted air pollution control, especially BC reduction, is crucial to mitigate associated health burdens.
{"title":"Roles of long-term exposure to ambient PM2.5 mass and its chemical components in the trajectory of chronic disease multimorbidity: Evidence from a large longitudinal study","authors":"Xinjie Xiao , Wei Wu , Juanjuan Zhang , Qijiong Zhu , Yilin Li , Yayi Li , Haoyi Feng , Wan Peng , Jianxiong Hu , Dan Cai , Hongwei Tu , Guanhao He , Wenjun Ma , Tao Liu","doi":"10.1016/j.hazadv.2025.100959","DOIUrl":"10.1016/j.hazadv.2025.100959","url":null,"abstract":"<div><div>Against the backdrop of global aging, rising risks of chronic diseases and multimorbidity pose considerable public health challenges. To investigate the association of long-term exposure to fine particulate matter (PM<sub>2.5</sub>) and its chemical components with multimorbidity development, this prospective cohort study included 8,257 participants from the China Health and Retirement Longitudinal Study (CHARLS) cohort (2011–2020). PM<sub>2.5</sub> mass and its chemical components (sulfate [SO<sub>4</sub><sup>2-</sup>], nitrate [NO<sub>3</sub><sup>-</sup>], ammonium [NH<sub>4</sub><sup>+</sup>], organic matter [OM], and black carbon [BC]) were evaluated by city-level three-year average exposures. Multistate models were used to estimate the hazard ratios (HRs) for chronic disease accumulation and death, and the corresponding population-attributable fractions (PAFs) attributable to PM<sub>2.5</sub> mass and its chemical components were also calculated. For single chronic disease patients, each standard deviation (SD = 14.2 μg/m³) increase in PM<sub>2.5</sub> mass concentration was associated with HRs of 1.46 and 2.14 for basic multimorbidity and death, respectively. Among those with basic multimorbidity, each SD increase yielded HRs of 1.31 for complex multimorbidity and 2.20 for death. BC showed the strongest association with multimorbidity development, followed by SO<sub>4</sub><sup>2-</sup>, OM, NH<sub>4</sub><sup>+</sup>, and NO<sub>3</sub><sup>-</sup>. Achieving China's Grade II PM<sub>2.5</sub> standard (35 μg/m³) could avert 19.32% of transitions from one disease to basic multimorbidity and 13.86% of transitions from basic to complex multimorbidity. Long-term exposure to PM<sub>2.5</sub> mass and its chemical components was associated with increased risks across all disease stages of multimorbidity development. Targeted air pollution control, especially BC reduction, is crucial to mitigate associated health burdens.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100959"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685540","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-01-24DOI: 10.1016/j.hazadv.2026.101036
Luke A. Gurtowski , Sheila J. McLeod , Sarah Grace Zetterholm , Chris S. Griggs , Josh Gramm , Jaylen Davis , Florence Sanchez
Graphene nanoplatelets (GnPs) were evaluated against munitions compounds 2,4,6-trinitrotoluene (TNT) and hexahydro-1,3,5-trinitro-s-triazine (RDX) in aqueous solutions for adsorptive removal performance. Fourier transform infrared and Raman spectroscopy were employed to characterize samples and inform adsorption mechanisms. Adsorption kinetics and isotherm studies were conducted in deionized water and compared with granular activated carbon (GAC). Evaluations were conducted with varying pH levels, ionic strengths, and temperatures and with surface water solutions to assess the impact of environmental factors on performance and further inform adsorption mechanisms. This study demonstrated that GnPs exhibited more rapid adsorption than GAC. Furthermore, TNT was adsorbed with greater capacity by GnPs compared to GAC, while GnPs removed RDX in greater capacity only when results were normalized for surface area. The more planar structure of GnPs may have contributed to performance enhancements relative to GAC. Adsorption was not impacted by variations in pH or ionic strength, indicating stable performance in different environments. Thermodynamic analysis indicated that removal was more favorable at higher temperatures. Furthermore, π-π interactions likely facilitated TNT removal by GnPs, while RDX was removed through physisorption by van der Waals forces. This study advanced understanding of environmental management of munitions compounds, as the adsorptive performance of GnPs for munitions compounds in solutions within a natural environmental matrix were evaluated, and key mechanisms supporting adsorptive removal of these compounds were informed. Overall, this study demonstrated the effectiveness of GnPs in treating water contaminated with TNT or RDX, particularly when rapid adsorption is preferred.
{"title":"Investigation of graphene nanoplatelets for adsorptive removal of aqueous munitions compounds 2,4,6-trinitrotoluene (TNT) and Hexahydro-1,3,5-trinitro-s-triazine (RDX)","authors":"Luke A. Gurtowski , Sheila J. McLeod , Sarah Grace Zetterholm , Chris S. Griggs , Josh Gramm , Jaylen Davis , Florence Sanchez","doi":"10.1016/j.hazadv.2026.101036","DOIUrl":"10.1016/j.hazadv.2026.101036","url":null,"abstract":"<div><div>Graphene nanoplatelets (GnPs) were evaluated against munitions compounds 2,4,6-trinitrotoluene (TNT) and hexahydro-1,3,5-trinitro-s-triazine (RDX) in aqueous solutions for adsorptive removal performance. Fourier transform infrared and Raman spectroscopy were employed to characterize samples and inform adsorption mechanisms. Adsorption kinetics and isotherm studies were conducted in deionized water and compared with granular activated carbon (GAC). Evaluations were conducted with varying pH levels, ionic strengths, and temperatures and with surface water solutions to assess the impact of environmental factors on performance and further inform adsorption mechanisms. This study demonstrated that GnPs exhibited more rapid adsorption than GAC. Furthermore, TNT was adsorbed with greater capacity by GnPs compared to GAC, while GnPs removed RDX in greater capacity only when results were normalized for surface area. The more planar structure of GnPs may have contributed to performance enhancements relative to GAC. Adsorption was not impacted by variations in pH or ionic strength, indicating stable performance in different environments. Thermodynamic analysis indicated that removal was more favorable at higher temperatures. Furthermore, π-π interactions likely facilitated TNT removal by GnPs, while RDX was removed through physisorption by van der Waals forces. This study advanced understanding of environmental management of munitions compounds, as the adsorptive performance of GnPs for munitions compounds in solutions within a natural environmental matrix were evaluated, and key mechanisms supporting adsorptive removal of these compounds were informed. Overall, this study demonstrated the effectiveness of GnPs in treating water contaminated with TNT or RDX, particularly when rapid adsorption is preferred.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 101036"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146077166","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Anemia is a significant global health problem, particularly affecting women and children. This study investigates the correlation between ambient fine particulate matter (PM2.5) exposure, access to clean household fuels, and anemia prevalence in vulnerable populations across 122 countries. This ecological study conducted an analysis using national-level data from 122 countries to examine the correlation between PM2.5 (in 2 years 2016 and 2019) and the percentage of the population with access to clean cooking fuels at the same time, along with three outcomes, including anemia prevalence in women of reproductive age (15–49 years), pregnant women, and children (6–59 months). Multiple linear regression was used to identify significant factors associated with anemia in these groups. Scatter plots illustrated how anemia prevalence varied across countries with air pollution, the Human Development Index (HDI), and the Socio-Demographic Index (SDI), highlighting the interplay between environmental and socio-economic factors. The positive association was observed between PM₂.₅ and anemia prevalence among non-pregnant women (β=0.16, P=0.001). Similar positive associations were observed for pregnant women (β=0.12, P=0.008) and children under five (β=0.182, P=0.001). Conversely, there was negative association between access to clean cooking and anemia prevalence among pregnant women (β = -0.23, p ≤ 0.001). Similar negative association was observed among children under five (β = -0.108, p =0.011). Results were consistent across exposure years (2016, 2019). These findings indicate that exposure to PM₂.₅ and limited access to clean fuel are significantly associated with increased anemia prevalence among women and children worldwide, independent of socioeconomic development. These findings underscore the importance of incorporating environmental factors, particularly air pollution, into public health strategies aimed at reducing anemia, especially in low- and middle-income countries.
{"title":"Global air pollution and clean fuel access to anemia burden in vulnerable populations","authors":"Reza Mosaddegh , Najmeh Zarei Jelyani , Saeid Gholami Gharab , Alireza Eshghi , Nilufar Marufi , Sara Naderpour , Saeedeh Askari , Mitra Gholami , Rozhan Khezri , Fatemeh Rezaei","doi":"10.1016/j.hazadv.2025.101000","DOIUrl":"10.1016/j.hazadv.2025.101000","url":null,"abstract":"<div><div>Anemia is a significant global health problem, particularly affecting women and children. This study investigates the correlation between ambient fine particulate matter (PM<sub>2.5</sub>) exposure, access to clean household fuels, and anemia prevalence in vulnerable populations across 122 countries. This ecological study conducted an analysis using national-level data from 122 countries to examine the correlation between PM<sub>2.5</sub> (in 2 years 2016 and 2019) and the percentage of the population with access to clean cooking fuels at the same time, along with three outcomes, including anemia prevalence in women of reproductive age (15–49 years), pregnant women, and children (6–59 months). Multiple linear regression was used to identify significant factors associated with anemia in these groups. Scatter plots illustrated how anemia prevalence varied across countries with air pollution, the Human Development Index (HDI), and the Socio-Demographic Index (SDI), highlighting the interplay between environmental and socio-economic factors. The positive association was observed between PM₂.₅ and anemia prevalence among non-pregnant women (β=0.16, P=0.001). Similar positive associations were observed for pregnant women (β=0.12, P=0.008) and children under five (β=0.182, P=0.001). Conversely, there was negative association between access to clean cooking and anemia prevalence among pregnant women (β = -0.23, p ≤ 0.001). Similar negative association was observed among children under five (β = -0.108, p =0.011). Results were consistent across exposure years (2016, 2019). These findings indicate that exposure to PM₂.₅ and limited access to clean fuel are significantly associated with increased anemia prevalence among women and children worldwide, independent of socioeconomic development. These findings underscore the importance of incorporating environmental factors, particularly air pollution, into public health strategies aimed at reducing anemia, especially in low- and middle-income countries.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 101000"},"PeriodicalIF":7.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146077172","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}