Pub Date : 2024-01-01DOI: 10.1016/j.enceco.2024.07.007
Chang-Yu Weng , Shi-Ming Jia , De-Qi Wang , Wan-Li Ma
The ecological and human health risks associated with heavy metal(loid)s (HMs) have attracted much attentions worldwide. In this study, 153 topsoil samples were collected across China in 2019, aiming to investigate the HMs pollution characteristics. The soil samples were collected from areas such as parks, schools, communities, and rural regions, which were far away from pollution sources of HMs. In order to study the temporal trend of pollution, related studies from 2000 to 2015 in China were also summarized. The findings indicated that Cd, Cu, Zn, and Pb were the major HMs with the mean concentrations of Cd, Cu, Zn, and Pb were 0.40, 36.5, 107, and 33.5 mg/kg, respectively. High background values and metal processing resulted in high total concentrations of Cd, As, Cr, and V especially in Southwest China (such as Guizhou and Yunnan provinces). The result of the Positive Matrix Factorization (PMF) model indicated the primary source of HMs was natural source (45.3%), followed by traffic source (20.6%), industrial source (17.3%), and agricultural source (16.8%). The health risk assessment of HMs indicated that non-carcinogenic risks were minimal, however, carcinogenic risks (95th) for As, Cr, and Cd should attract attentions. Compared with the measurements from 2000 to 2015, the pollution levels of HMs showed a decreasing trend in China in 2019, which indicated the effectives on HMs control along with the implementation of the control policy on soil in China.
重金属(HMs)对生态和人类健康的危害在全球范围内备受关注。本研究于 2019 年在全国范围内采集了 153 个表层土壤样品,旨在研究 HMs 的污染特征。土壤样品采集于远离 HMs 污染源的公园、学校、社区、农村等区域。为了研究污染的时间趋势,还总结了 2000 年至 2015 年中国的相关研究。研究结果表明,镉、铜、锌和铅是主要的有害物质,镉、铜、锌和铅的平均浓度分别为 0.40、36.5、107 和 33.5 毫克/千克。高背景值和金属加工导致镉、砷、铬和钒的总浓度较高,尤其是在中国西南地区(如贵州省和云南省)。正矩阵因式分解(PMF)模型的结果表明,HMs 的主要来源是自然源(45.3%),其次是交通源(20.6%)、工业源(17.3%)和农业源(16.8%)。HMs 的健康风险评估结果表明,非致癌风险极低,但 As、Cr 和 Cd 的致癌风险(第 95 位)值得关注。与 2000 年至 2015 年的测量结果相比,2019 年中国的 HMs 污染水平呈下降趋势,这表明随着中国土壤控制政策的实施,HMs 控制取得了成效。
{"title":"Pollution characteristics of heavy metal(loid)s in soil in China: Implications for health risk assessment and temporal trend analysis","authors":"Chang-Yu Weng , Shi-Ming Jia , De-Qi Wang , Wan-Li Ma","doi":"10.1016/j.enceco.2024.07.007","DOIUrl":"10.1016/j.enceco.2024.07.007","url":null,"abstract":"<div><p>The ecological and human health risks associated with heavy metal(loid)s (HMs) have attracted much attentions worldwide. In this study, 153 topsoil samples were collected across China in 2019, aiming to investigate the HMs pollution characteristics. The soil samples were collected from areas such as parks, schools, communities, and rural regions, which were far away from pollution sources of HMs. In order to study the temporal trend of pollution, related studies from 2000 to 2015 in China were also summarized. The findings indicated that Cd, Cu, Zn, and Pb were the major HMs with the mean concentrations of Cd, Cu, Zn, and Pb were 0.40, 36.5, 107, and 33.5 mg/kg, respectively. High background values and metal processing resulted in high total concentrations of Cd, As, Cr, and V especially in Southwest China (such as Guizhou and Yunnan provinces). The result of the Positive Matrix Factorization (PMF) model indicated the primary source of HMs was natural source (45.3%), followed by traffic source (20.6%), industrial source (17.3%), and agricultural source (16.8%). The health risk assessment of HMs indicated that non-carcinogenic risks were minimal, however, carcinogenic risks (95th) for As, Cr, and Cd should attract attentions. Compared with the measurements from 2000 to 2015, the pollution levels of HMs showed a decreasing trend in China in 2019, which indicated the effectives on HMs control along with the implementation of the control policy on soil in China.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 248-258"},"PeriodicalIF":9.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590182624000286/pdfft?md5=d74e835bb2665d87e0ffc8ef2e5cb122&pid=1-s2.0-S2590182624000286-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141960280","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-01DOI: 10.1016/j.enceco.2024.07.006
Ajibola A. Bayode , Stephen Sunday Emmanuel , Saheed O. Sanni , Olamide A. Olalekan , Odunayo Timothy Ore , Daniel Terlanga Koko , Martins O. Omorogie
Micropollutants such as steroid hormones contaminate water worldwide and cause significant damage. Wastewater treatment plants (WWTPs) partially remove them, and they have low biodegradability leading to their persistence in water bodies. They are endocrine disruptor compounds in aquatic organisms. Various environmental conditions contribute to their persistence in the environment like soil pH, organic matter, soil conditions, and temperature. The aquatic environment is most threatened even when present at very low concentrations. The environment is exposed to steroid hormones from agricultural run-offs, pharmaceutical and industrial waste, and veterinary medicine. Since most WWTPs partially remove contaminants, there is a need for new and improved technologies for higher and more efficient removal of steroid hormones.
This paper discusses the fate and toxicity of steroid hormones in the aquatic environment. It further elucidates the existing and emerging technologies in the treatment of steroid hormones in aquatic environments. Finally, the conclusion of this review along with the current limitations and future research perspectives of hormones present in the environment are elucidated.
{"title":"Current status and performance evaluation of emerging advanced remediation techniques for the removal of steroidal hormones in water","authors":"Ajibola A. Bayode , Stephen Sunday Emmanuel , Saheed O. Sanni , Olamide A. Olalekan , Odunayo Timothy Ore , Daniel Terlanga Koko , Martins O. Omorogie","doi":"10.1016/j.enceco.2024.07.006","DOIUrl":"10.1016/j.enceco.2024.07.006","url":null,"abstract":"<div><p>Micropollutants such as steroid hormones contaminate water worldwide and cause significant damage. Wastewater treatment plants (WWTPs) partially remove them, and they have low biodegradability leading to their persistence in water bodies. They are endocrine disruptor compounds in aquatic organisms. Various environmental conditions contribute to their persistence in the environment like soil pH, organic matter, soil conditions, and temperature. The aquatic environment is most threatened even when present at very low concentrations. The environment is exposed to steroid hormones from agricultural run-offs, pharmaceutical and industrial waste, and veterinary medicine. Since most WWTPs partially remove contaminants, there is a need for new and improved technologies for higher and more efficient removal of steroid hormones.</p><p>This paper discusses the fate and toxicity of steroid hormones in the aquatic environment. It further elucidates the existing and emerging technologies in the treatment of steroid hormones in aquatic environments. Finally, the conclusion of this review along with the current limitations and future research perspectives of hormones present in the environment are elucidated.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 315-337"},"PeriodicalIF":9.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590182624000274/pdfft?md5=efbaff2ec1b880805924e59bf21b9845&pid=1-s2.0-S2590182624000274-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141840520","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-01DOI: 10.1016/j.enceco.2024.07.008
Ahsan Shah , Georgina Manning , Julia Zakharova , Arun Arjunan , Maryam Batool , Alisha J. Hawkins
The treatment of drinking water using Moringa oleifera (MO) Lam. seeds is gaining popularity as a sustainable alternative to synthetic chemicals. However, there is limited literature on the effect of particle size of the ground MO seeds on their coagulation characteristics, which is revealed in this study. To investigate the impact of the particle size, the sun-dried MO seeds were ground and sieved into five distinct sizes ranging from (i) <0.25 mm, (ii) 0.25–0.4 mm, (iii) 0.4–0.8 mm, (iv) 0.8–1.25 mm, and (v) 1.25–2.0 mm. The seed protein for the experiment was then prepared by stirring a 2% (w/v) solution of the five different seed powders in tap water. Six different protein doses between 100 and 350 mg/l were added to separate glass beakers featuring a synthetic solution of 80 nephelometric turbidity units (NTU) turbidity. The experimental results revealed that the MO seed particle sizes of 0.8–0.4 mm and 0.4–0.25 mm demonstrated superior coagulation characteristics compared to the other size categories tested. Specifically, a dose of 200–300 mg/l was found to be effective in reducing the turbidity to 5 NTU and eliminating 100% of E. coli after 3 h of settling. The surface characterisation showed a heterogenous surface and the presence of functional groups, which may have aided coagulation and caused the reduction in turbidity and microbial load. Statistical analysis revealed a P value <0.05, indicating that the results were highly consistent with no >5% variation. The study is also extended to explore the mechanism of coagulation of MO seeds, and the potential application of the research at a domestic scale is also discussed. Overall, the resulting water treated with MO met the WHO criteria.
使用油辣木籽(Moringa oleifera (MO) Lam.)处理饮用水作为合成化学品的可持续替代品正日益受到欢迎。然而,关于磨碎的 MO 种子的粒度对其凝结特性的影响的文献却很有限,本研究揭示了这一点。为了研究粒度的影响,将晒干的 MO 种子研磨并筛分成五种不同的粒度,分别为 (i) <0.25 mm、(ii) 0.25-0.4 mm、(iii) 0.4-0.8 mm、(iv) 0.8-1.25 mm 和 (v) 1.25-2.0 mm。然后,将五种不同种子粉末的 2%(w/v)溶液在自来水中搅拌,制备实验所需的种子蛋白质。将 100 至 350 毫克/升的六种不同剂量的蛋白质分别加入具有 80 尼菲尔浊度单位(NTU)浊度的合成溶液的玻璃烧杯中。实验结果表明,MO 种子粒径为 0.8-0.4 毫米和 0.4-0.25 毫米的混凝特性优于其他粒径类别。具体来说,200-300 毫克/升的剂量可有效地将浊度降低到 5 NTU,并在沉淀 3 小时后去除 ∼100% 的大肠杆菌。表面特性分析表明,表面具有异质性并存在功能基团,这可能有助于凝结,并导致浊度和微生物负荷的降低。统计分析显示,P 值为 0.05,表明结果高度一致,没有 5% 的差异。研究还扩展到探索 MO 种子的混凝机理,并讨论了该研究在家庭规模上的潜在应用。总体而言,经 MO 处理后的水符合世界卫生组织的标准。
{"title":"Particle size effect of Moringa oleifera Lam. seeds on the turbidity removal and antibacterial activity for drinking water treatment","authors":"Ahsan Shah , Georgina Manning , Julia Zakharova , Arun Arjunan , Maryam Batool , Alisha J. Hawkins","doi":"10.1016/j.enceco.2024.07.008","DOIUrl":"10.1016/j.enceco.2024.07.008","url":null,"abstract":"<div><p>The treatment of drinking water using <em>Moringa oleifera</em> (MO) Lam. seeds is gaining popularity as a sustainable alternative to synthetic chemicals. However, there is limited literature on the effect of particle size of the ground MO seeds on their coagulation characteristics, which is revealed in this study. To investigate the impact of the particle size, the sun-dried MO seeds were ground and sieved into five distinct sizes ranging from (<em>i</em>) <0.25 mm, (<em>ii</em>) 0.25–0.4 mm, (<em>iii</em>) 0.4–0.8 mm, (<em>iv</em>) 0.8–1.25 mm, and (<em>v</em>) 1.25–2.0 mm. The seed protein for the experiment was then prepared by stirring a 2% (<em>w</em>/<em>v</em>) solution of the five different seed powders in tap water. Six different protein doses between 100 and 350 mg/l were added to separate glass beakers featuring a synthetic solution of 80 nephelometric turbidity units (NTU) turbidity. The experimental results revealed that the MO seed particle sizes of 0.8–0.4 mm and 0.4–0.25 mm demonstrated superior coagulation characteristics compared to the other size categories tested. Specifically, a dose of 200–300 mg/l was found to be effective in reducing the turbidity to 5 NTU and eliminating <span><math><mo>∼</mo></math></span>100% of <em>E. coli</em> after 3 h of settling. The surface characterisation showed a heterogenous surface and the presence of functional groups, which may have aided coagulation and caused the reduction in turbidity and microbial load. Statistical analysis revealed a <em>P</em> value <0.05, indicating that the results were highly consistent with no >5% variation. The study is also extended to explore the mechanism of coagulation of MO seeds, and the potential application of the research at a domestic scale is also discussed. Overall, the resulting water treated with MO met the WHO criteria.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 370-379"},"PeriodicalIF":9.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590182624000298/pdfft?md5=573b608148f7978a0d975d7e0004cb98&pid=1-s2.0-S2590182624000298-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141847373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Microbial biodegradation of oil pollutants and their derivatives has become the most environmental-friendly method in the developing world. The aim of this study was to evaluate crude oil biodegradation potential of lipase produced by indigenous bacteria from oil contaminated soil. Indigenous bacteria isolates were identified as species of Bacillus subtilis and Pseudomonas aeruginosa, the isolates were able to produce lipase as revealed in their zone of clearance on tween 80 agar plates and the presence of lipase produced by the two bacteria were further confirmed using spectrophotometric analyses. Lipase produced by B. subtilis showed maximal lipase activity at pH 8 and 40 while the enzyme produced by P. aeruginosa showed maximal lipase activity (U/mL) at pH 8 and 50 when subjected to various pH and temperature respectively. Lipase produced by B. subtilis recorded 8.11 ± 0.70 of crude oil degradation in mineral salt medium within 28 days, while that of P. aeruginosa recorded 15.6 ± 0.03 of crude oil biodegradation. The GC–MS analysis of the crude oil treatment showed complete mineralization of several compounds, and also showed peak reduction which indicates lipase efficiency in the degradation of hydrocarbons. As revealed by GC–MS analysis, out of the 8 hydrocarbons identified in an undegraded oil, 5 were completely degraded by the enzyme activities while 2 (toluene and methyl, cyclopentane) were identified with hydrocarbons treated with lipase. The enzymes produced by B. subtilis and P. aeruginosa can serve as useful product for bioremediation of crude oil contaminated soil.
{"title":"Crude oil biodegradation potential of lipase produced by Bacillus subtilis and Pseudomonas aeruginosa isolated from hydrocarbon contaminated soil","authors":"A. Abubakar , O.P. Abioye , S.A. Aransiola , Naga Raju Maddela , Ram Prasad","doi":"10.1016/j.enceco.2023.12.001","DOIUrl":"10.1016/j.enceco.2023.12.001","url":null,"abstract":"<div><p>Microbial biodegradation of oil pollutants and their derivatives has become the most environmental-friendly method in the developing world. The aim of this study was to evaluate crude oil biodegradation potential of lipase produced by indigenous bacteria from oil contaminated soil. Indigenous bacteria isolates were identified as species of <em>Bacillus subtilis</em> and <em>Pseudomonas aeruginosa</em>, the isolates were able to produce lipase as revealed in their zone of clearance on tween 80 agar plates and the presence of lipase produced by the two bacteria were further confirmed using spectrophotometric analyses. Lipase produced by <em>B. subtilis</em> showed maximal lipase activity at pH 8 and 40<span><math><mo>°</mo><mi>C</mi></math></span> while the enzyme produced by <em>P. aeruginosa</em> showed maximal lipase activity (U/mL) at pH 8 and 50<span><math><mo>°</mo><mi>C</mi></math></span> when subjected to various pH and temperature respectively. Lipase produced by <em>B. subtilis</em> recorded 8.11 ± 0.70<span><math><mo>%</mo></math></span> of crude oil degradation in mineral salt medium within 28 days, while that of <em>P. aeruginosa</em> recorded 15.6 ± 0.03<span><math><mo>%</mo></math></span> of crude oil biodegradation. The GC–MS analysis of the crude oil treatment showed complete mineralization of several compounds, and also showed peak reduction which indicates lipase efficiency in the degradation of hydrocarbons. As revealed by GC–MS analysis, out of the 8 hydrocarbons identified in an undegraded oil, 5 were completely degraded by the enzyme activities while 2 (toluene and methyl, cyclopentane) were identified with hydrocarbons treated with lipase. The enzymes produced by <em>B. subtilis</em> and <em>P. aeruginosa</em> can serve as useful product for bioremediation of crude oil contaminated soil.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 26-32"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590182623000292/pdfft?md5=1ac5c4bcaa4c0b27e9822b7e7074a1c9&pid=1-s2.0-S2590182623000292-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139393991","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-01DOI: 10.1016/j.enceco.2024.08.006
Yuan-Wei Zhang , Dong-Yang Zhou , Si-Cheng Wang , Feng-Jin Zhou , Guang-Chao Wang , Jia-Can Su
Microplastics are widespread pollutants in the environment, with characteristics such as small particle size, strong adsorption, and difficult degradation, and have gradually become a global pollution problem, potentially endangering host health via various mechanisms. Currently, numerous research has verified biological toxic effects of microplastics in a variety of organisms and human organs and tissues, while the understanding of interaction between microplastics and bone metabolism is still limited. Based on assessing the relevance between microplastics and bone metabolism, strengthening the monitoring and control of microplastic pollution, and clarifying the mechanisms of microplastics on the bone metabolism, is critical for prevention and treatment of bone metabolic diseases. Herein, this review summarizes the classification of microplastics, source and distribution of microplastics, pathways of microplastics invading host, impacts and mechanisms of microplastics modulating the bone metabolism, and potential recommendations for preventing bone metabolic diseases caused by microplastic invasion, thus providing a novel perspective for the in-depth exploration of microplastics on bone metabolism and pivotal references for the future related researches and health policy formulation.
{"title":"Bridging relevance between microplastics, human health and bone metabolism: Emerging threats and research directions","authors":"Yuan-Wei Zhang , Dong-Yang Zhou , Si-Cheng Wang , Feng-Jin Zhou , Guang-Chao Wang , Jia-Can Su","doi":"10.1016/j.enceco.2024.08.006","DOIUrl":"10.1016/j.enceco.2024.08.006","url":null,"abstract":"<div><p>Microplastics are widespread pollutants in the environment, with characteristics such as small particle size, strong adsorption, and difficult degradation, and have gradually become a global pollution problem, potentially endangering host health via various mechanisms. Currently, numerous research has verified biological toxic effects of microplastics in a variety of organisms and human organs and tissues, while the understanding of interaction between microplastics and bone metabolism is still limited. Based on assessing the relevance between microplastics and bone metabolism, strengthening the monitoring and control of microplastic pollution, and clarifying the mechanisms of microplastics on the bone metabolism, is critical for prevention and treatment of bone metabolic diseases. Herein, this review summarizes the classification of microplastics, source and distribution of microplastics, pathways of microplastics invading host, impacts and mechanisms of microplastics modulating the bone metabolism, and potential recommendations for preventing bone metabolic diseases caused by microplastic invasion, thus providing a novel perspective for the in-depth exploration of microplastics on bone metabolism and pivotal references for the future related researches and health policy formulation.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 422-435"},"PeriodicalIF":9.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590182624000365/pdfft?md5=45d69c7db0773b73a3b12fe6e419d0a5&pid=1-s2.0-S2590182624000365-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142232000","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Environmental toxins threaten human health and ecosystem integrity, necessitating advanced detection, degradation, and removal methodologies. In recent years, the scientific community has increasingly focused on MXenes, a novel class of two-dimensional (2D) transition metal carbides, nitrides, and carbonitrides, due to their exceptional potential in toxin management. This comprehensive review thoroughly examines MXenes, including synthesis methods, structural and chemical properties, and functionalization strategies. Unique to this review is the integrated discussion of MXenes in the context of environmental toxin management, encompassing detection, degradation, and removal within a single study. The enhancement of sensor technologies using MXenes for rapid and precise toxin detection is thoroughly analyzed. It focuses on MXene-mediated degradation pathways, especially photocatalytic and electrocatalytic mechanisms, considering their redox potential and light-harvesting capabilities. Additionally, the adsorption dynamics of MXene-based adsorbents are scrutinized, covering adsorption capacity, kinetics, and regeneration/recyclability. The review offers a comparative evaluation of MXenes with other 2D materials, positioning MXenes within the broader context of toxin management solutions. This article stands out for its novel and comprehensive approach, being the first to concurrently address the detection, degradation, and removal of environmental toxins using MXenes. The review concludes by underscoring the vast potential of MXenes in addressing environmental toxins. It emphasizes the urgent need for continued research to optimize their performance, scale up production, and enable practical implementation. This detailed reference aims to serve researchers and practitioners in environmental management, guiding future innovations and applications of MXenes in toxin control.
{"title":"Two-dimensional MXenes for toxin management: Advanced electrocatalytic detection, degradation, and adsorption dynamics","authors":"Sakthivel Kogularasu , Yung-Lung Chen , Yen-Yi Lee , Bo-Wun Huang , Perumal Murugesan , Guo-Ping Chang-Chien , Mani Govindasamy","doi":"10.1016/j.enceco.2024.08.005","DOIUrl":"10.1016/j.enceco.2024.08.005","url":null,"abstract":"<div><p>Environmental toxins threaten human health and ecosystem integrity, necessitating advanced detection, degradation, and removal methodologies. In recent years, the scientific community has increasingly focused on MXenes, a novel class of two-dimensional (2D) transition metal carbides, nitrides, and carbonitrides, due to their exceptional potential in toxin management. This comprehensive review thoroughly examines MXenes, including synthesis methods, structural and chemical properties, and functionalization strategies. Unique to this review is the integrated discussion of MXenes in the context of environmental toxin management, encompassing detection, degradation, and removal within a single study. The enhancement of sensor technologies using MXenes for rapid and precise toxin detection is thoroughly analyzed. It focuses on MXene-mediated degradation pathways, especially photocatalytic and electrocatalytic mechanisms, considering their redox potential and light-harvesting capabilities. Additionally, the adsorption dynamics of MXene-based adsorbents are scrutinized, covering adsorption capacity, kinetics, and regeneration/recyclability. The review offers a comparative evaluation of MXenes with other 2D materials, positioning MXenes within the broader context of toxin management solutions. This article stands out for its novel and comprehensive approach, being the first to concurrently address the detection, degradation, and removal of environmental toxins using MXenes. The review concludes by underscoring the vast potential of MXenes in addressing environmental toxins. It emphasizes the urgent need for continued research to optimize their performance, scale up production, and enable practical implementation. This detailed reference aims to serve researchers and practitioners in environmental management, guiding future innovations and applications of MXenes in toxin control.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 390-407"},"PeriodicalIF":9.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590182624000353/pdfft?md5=9bc26f736be11514cb54556eeff8e338&pid=1-s2.0-S2590182624000353-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142129152","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-01DOI: 10.1016/j.enceco.2024.01.002
Anwuli U. Osadebe , Chimezie J. Ogugbue , Gideon C. Okpokwasili
Nutrient washout remains a key drawback of nutrient supplementation during bioremediation interventions in aquatic systems. This study assessed the adsorption and controlled release properties of biochar‑iron oxide nanoparticle (IONPs) beads laden with bacteria and nutrients for treatment of petroleum spills in freshwater ecosystems in a bid to counter the challenge of nutrient washout. The IONPs synthesised from phytoextracts were decorated on biochar made from cow bones at 500 °C. The composite produced was embedded in an alginate matrix with degradative bacteria and inorganic nutrients via physical crosslinking. Swelling indices revealed better release properties for the monoammonium phosphate nutrients with the beads that had the biochar‑iron oxide nanocomposite incorporated (BCNP). The 15-min swelling indices (SI15) for the beads ranged from 0.13 to 2.00. Batch adsorption experiments revealed that adsorption was physical in nature and higher at lower adsorbate concentrations with significant differences (p ≤ 0.05) between the three groups of adsorbents. The BCNP bead showed the greatest sorption levels (71.69%) compared to the plain biochar beads (57.83%) and the biochar powder (46.12%). Based on the adsorption parameters obtained, it was concluded that the adsorption data were more suited to the Freundlich isotherm model and the pseudo-second order kinetic model. The study developed a slow-release nanocomposite that could counter the challenge of nutrient washout associated with bioremediation in aquatic ecosystems.
{"title":"Biochar and Iron oxide nanoparticle-impregnated alginate beads as adsorbents for enhanced ex situ bioremediation of petroleum-contaminated freshwater","authors":"Anwuli U. Osadebe , Chimezie J. Ogugbue , Gideon C. Okpokwasili","doi":"10.1016/j.enceco.2024.01.002","DOIUrl":"10.1016/j.enceco.2024.01.002","url":null,"abstract":"<div><p>Nutrient washout remains a key drawback of nutrient supplementation during bioremediation interventions in aquatic systems. This study assessed the adsorption and controlled release properties of biochar‑iron oxide nanoparticle (IONPs) beads laden with bacteria and nutrients for treatment of petroleum spills in freshwater ecosystems in a bid to counter the challenge of nutrient washout. The IONPs synthesised from phytoextracts were decorated on biochar made from cow bones at 500 °C. The composite produced was embedded in an alginate matrix with degradative bacteria and inorganic nutrients via physical crosslinking. Swelling indices revealed better release properties for the monoammonium phosphate nutrients with the beads that had the biochar‑iron oxide nanocomposite incorporated (BCNP). The 15-min swelling indices (SI<sub>15</sub>) for the beads ranged from 0.13 to 2.00. Batch adsorption experiments revealed that adsorption was physical in nature and higher at lower adsorbate concentrations with significant differences (<em>p</em> ≤ 0.05) between the three groups of adsorbents. The BCNP bead showed the greatest sorption levels (71.69%) compared to the plain biochar beads (57.83%) and the biochar powder (46.12%). Based on the adsorption parameters obtained, it was concluded that the adsorption data were more suited to the Freundlich isotherm model and the pseudo-second order kinetic model. The study developed a slow-release nanocomposite that could counter the challenge of nutrient washout associated with bioremediation in aquatic ecosystems.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 42-50"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S259018262400002X/pdfft?md5=a9ee5e4bb6089f9204d1f10803ade3ca&pid=1-s2.0-S259018262400002X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139633383","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This study is an attempt to assess the influence of the oil storage depot discharges on proximate water sources in Ibadan, southwest Nigeria. Fifteen priority polycyclic aromatic hydrocarbons (PAHs) were examined in a total of 15 water samples (10 groundwater +4 surface water samples) utilizing gas chromatography–mass spectrometry, after extraction of the waters with dichloromethane and clean-up of the extracts. Results revealed that values of overall PAHs in groundwater (GW) and surface water (SW) varied from 0.01 to 3.45 mg/L (mean = 0.42 mg/L) and 0.01 to 0.09 mg/L (mean = 0.05 mg/L), correspondingly. The highest value of ∑15 PAHs (3.45 mg/L) was observed at 24 m to the discharge point. The ring wise distribution pattern of the PAHs in collected water samples follows the order: 2–3 rings >5–6 rings >4 – ring PAHs and low molecular weight (LMW) PAHs accounted for 90.73% relative to HMW (9.27%) in groundwater samples. The diagnostic ratios suggested that the PAHs pollution in water were likely from incomplete combustion of fossil fuels, vehicle emissions and released petroleum effluents from nearby depot. The concentration of carcinogenic PAHs in GW and SW ranged from to mg/L and to mg/L, correspondingly, which highlights possible human health risks. The values of hazard index (HI) for the studied samples via the oral ingestion and dermal exposure pathways are less than unity, suggesting no adverse non-carcinogenic health effects. The calculated incremental lifetime cancer risk (ILCR) for adults and children are in the 10−2–10−3 range, implying noteworthy possible carcinogenic health effects to human beings, with children being the most susceptible. Correspondingly, dibenzo [a, h] anthracence (DahA) and Benzo [a] pyrene (BaP) were established to be of greater carcinogenic threats in the waters taken from the study location. The study advocates complete discontinuance of discharge release into the neighboring environment.
{"title":"Levels, distribution, origins, and human health risk evaluation of polycyclic aromatic hydrocarbons in groundwater around a petroleum depot wastewater discharge point","authors":"S.A. Ganiyu , A.E. Komolafe , K.A. Basheeru , R.A. Lasisi , A.A. Adeyemi","doi":"10.1016/j.enceco.2024.07.004","DOIUrl":"10.1016/j.enceco.2024.07.004","url":null,"abstract":"<div><p>This study is an attempt to assess the influence of the oil storage depot discharges on proximate water sources in Ibadan, southwest Nigeria. Fifteen priority polycyclic aromatic hydrocarbons (PAHs) were examined in a total of 15 water samples (10 groundwater +4 surface water samples) utilizing gas chromatography–mass spectrometry, after extraction of the waters with dichloromethane and clean-up of the extracts. Results revealed that values of overall PAHs in groundwater (GW) and surface water (SW) varied from 0.01 to 3.45 mg/L (mean = 0.42 mg/L) and 0.01 to 0.09 mg/L (mean = 0.05 mg/L), correspondingly. The highest value of ∑15 PAHs (3.45 mg/L) was observed at 24 m to the discharge point. The ring wise distribution pattern of the PAHs in collected water samples follows the order: 2–3 rings >5–6 rings >4 – ring PAHs and low molecular weight (LMW) PAHs accounted for 90.73% relative to HMW (9.27%) in groundwater samples. The diagnostic ratios suggested that the PAHs pollution in water were likely from incomplete combustion of fossil fuels, vehicle emissions and released petroleum effluents from nearby depot. The concentration of carcinogenic PAHs in GW and SW ranged from <span><math><mn>1</mn><mo>×</mo><msup><mn>10</mn><mrow><mo>−</mo><mn>2</mn></mrow></msup></math></span>to <span><math><mn>9</mn><mo>×</mo><msup><mn>10</mn><mrow><mo>−</mo><mn>2</mn></mrow></msup></math></span> mg/L and <span><math><mn>1</mn><mo>×</mo><msup><mn>10</mn><mrow><mo>−</mo><mn>2</mn></mrow></msup></math></span>to <span><math><mn>7</mn><mo>×</mo><msup><mn>10</mn><mrow><mo>−</mo><mn>2</mn></mrow></msup></math></span> mg/L, correspondingly, which highlights possible human health risks. The values of hazard index (HI) for the studied samples via the oral ingestion and dermal exposure pathways are less than unity, suggesting no adverse non-carcinogenic health effects. The calculated incremental lifetime cancer risk (ILCR) for adults and children are in the 10<sup>−2</sup>–10<sup>−3</sup> range, implying noteworthy possible carcinogenic health effects to human beings, with children being the most susceptible. Correspondingly, dibenzo [a, h] anthracence (DahA) and Benzo [a] pyrene (BaP) were established to be of greater carcinogenic threats in the waters taken from the study location. The study advocates complete discontinuance of discharge release into the neighboring environment.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 303-314"},"PeriodicalIF":9.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590182624000250/pdfft?md5=9765d6e97610c309817471801f9475c5&pid=1-s2.0-S2590182624000250-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141713324","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-01DOI: 10.1016/j.enceco.2024.04.002
Obey Gotore , Tirivashe Philip Masere , Macdonald Tatenda Muronda
The multifunctional properties of biochar make it a promising adsorbent of heavy metals for environmental bioremediation. Pyrolytic temperature is a key factor that impacts the properties, performance, and mechanisms of agro-wastes-derived biochar because of the physiochemical transformation of its structural composition. It has been deliberated that increased pyrolysis temperatures strongly enhance specific surface area, pH, and high microporosity as well as carbon and ash content with low cation exchange capacity and volatiles content. The reason for different properties from different pyrolysis is related to the variations in the lignin-cellulose structures as well as moistures in different agro-waste biomasses. Biochar has been considered a low-cost material that has shown its convenient applicability in rural areas of developing countries where environmental contamination of heavy metals is emerging. A wide range of pyrolytic temperatures has shown distinctive properties and characteristics of biochar from different biomass and their capacities to remove heavy metals. Higher pyrolysis temperatures can exhibit higher specific surface areas, enhanced functional groups, and stability than modified biochar. Different pyrolysis temperatures exhibited diverse adsorption capacities on biomass such as rice husk and corncob, as efficiency increases with temperatures on selective heavy metals such as hexavalent chromium [Cr(VI)], cadmium [Cd(II)] and zinc [Zn(II)]. This review aimed to understand the physiochemical and structural properties, and the transformation of pristine biochar that can enhance the environmental bioremediation of heavy metals. The deliberations on the mechanisms of diverse biomasses obtained from different pyrolysis for decision-making processes as well as production costs were reviewed. The authors propose future investigations on heavy metal immobilization to unlock the full potential of biochar in environmental bioremediation.
{"title":"The immobilization and adsorption mechanisms of agro-waste based biochar: A review on the effectiveness of pyrolytic temperatures on heavy metal removal","authors":"Obey Gotore , Tirivashe Philip Masere , Macdonald Tatenda Muronda","doi":"10.1016/j.enceco.2024.04.002","DOIUrl":"10.1016/j.enceco.2024.04.002","url":null,"abstract":"<div><p>The multifunctional properties of biochar make it a promising adsorbent of heavy metals for environmental bioremediation. Pyrolytic temperature is a key factor that impacts the properties, performance, and mechanisms of agro-wastes-derived biochar because of the physiochemical transformation of its structural composition. It has been deliberated that increased pyrolysis temperatures strongly enhance specific surface area, pH, and high microporosity as well as carbon and ash content with low cation exchange capacity and volatiles content. The reason for different properties from different pyrolysis is related to the variations in the lignin-cellulose structures as well as moistures in different agro-waste biomasses. Biochar has been considered a low-cost material that has shown its convenient applicability in rural areas of developing countries where environmental contamination of heavy metals is emerging. A wide range of pyrolytic temperatures has shown distinctive properties and characteristics of biochar from different biomass and their capacities to remove heavy metals. Higher pyrolysis temperatures can exhibit higher specific surface areas, enhanced functional groups, and stability than modified biochar. Different pyrolysis temperatures exhibited diverse adsorption capacities on biomass such as rice husk and corncob, as efficiency increases with temperatures on selective heavy metals such as hexavalent chromium [Cr(VI)], cadmium [Cd(II)] and zinc [Zn(II)]. This review aimed to understand the physiochemical and structural properties, and the transformation of pristine biochar that can enhance the environmental bioremediation of heavy metals. The deliberations on the mechanisms of diverse biomasses obtained from different pyrolysis for decision-making processes as well as production costs were reviewed. The authors propose future investigations on heavy metal immobilization to unlock the full potential of biochar in environmental bioremediation.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 92-103"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590182624000079/pdfft?md5=48777372c8beb679563bc4a0df9fe78a&pid=1-s2.0-S2590182624000079-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140787343","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The escalating production and ubiquitous presence of plastics and their degradation products, such as microplastics and nanoplastics, pose a significant environmental threat. Microplastics enter the soil through various pathways, including agricultural practices, plastic degradation, and wastewater disposal. Herein, we discussed the harmful effects of microplastics on the physicochemical properties of soil, plant growth, terrestrial fauna, and microbial activity, potentially affecting the stability and nutrient cycle of the soil ecosystem. This review delves into recent advances in potential microplastic bioremediation approaches, such as phytoremediation strategies utilized by plants and their associated microbes to accumulate, immobilize, and even degrade microplastics. Rhizosphere microorganisms play a crucial role in the degradation of microplastics, potentially utilizing them as a carbon source. Soil animals like earthworms, snails, and mealworms can also contribute significantly to bioremediation by ingesting and degrading microplastics through their gut microbiota. Various soil microorganisms, including bacteria and fungi, can degrade different microplastics with the help of enzymes such as laccase, esterase, peroxidase, oxidoreductase, and hydrolases and depolymerise the larger polymer chains into smaller units that ultimately mineralize them into CO2, H2O, and CH4. Genetic engineering and synthetic biology are also used to create strains with enhanced microplastic degrading and mineralization capabilities. It holds promise for efficient bioremediation but requires further research for real-world application and scalable implementation. Overall, this review comprehensively highlights the potential of bioremediation approaches and future recommendations for tackling microplastic pollution. Further research and development are crucial for enhancing biodegradation efficiency and scaling up this strategy for environmental protection.
{"title":"Potential strategies for bioremediation of microplastic contaminated soil","authors":"Charu Thapliyal , Anshu Priya , Salam Bhopen Singh , Vivekanand Bahuguna , Achlesh Daverey","doi":"10.1016/j.enceco.2024.05.001","DOIUrl":"https://doi.org/10.1016/j.enceco.2024.05.001","url":null,"abstract":"<div><p>The escalating production and ubiquitous presence of plastics and their degradation products, such as microplastics and nanoplastics, pose a significant environmental threat. Microplastics enter the soil through various pathways, including agricultural practices, plastic degradation, and wastewater disposal. Herein, we discussed the harmful effects of microplastics on the physicochemical properties of soil, plant growth, terrestrial fauna, and microbial activity, potentially affecting the stability and nutrient cycle of the soil ecosystem. This review delves into recent advances in potential microplastic bioremediation approaches, such as phytoremediation strategies utilized by plants and their associated microbes to accumulate, immobilize, and even degrade microplastics. Rhizosphere microorganisms play a crucial role in the degradation of microplastics, potentially utilizing them as a carbon source. Soil animals like earthworms, snails, and mealworms can also contribute significantly to bioremediation by ingesting and degrading microplastics through their gut microbiota. Various soil microorganisms, including bacteria and fungi, can degrade different microplastics with the help of enzymes such as laccase, esterase, peroxidase, oxidoreductase, and hydrolases and depolymerise the larger polymer chains into smaller units that ultimately mineralize them into CO<sub>2,</sub> H<sub>2</sub>O, and CH<sub>4</sub>. Genetic engineering and synthetic biology are also used to create strains with enhanced microplastic degrading and mineralization capabilities. It holds promise for efficient bioremediation but requires further research for real-world application and scalable implementation. Overall, this review comprehensively highlights the potential of bioremediation approaches and future recommendations for tackling microplastic pollution. Further research and development are crucial for enhancing biodegradation efficiency and scaling up this strategy for environmental protection.</p></div>","PeriodicalId":100480,"journal":{"name":"Environmental Chemistry and Ecotoxicology","volume":"6 ","pages":"Pages 117-131"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590182624000092/pdfft?md5=bf2f73c4a9132606f2abb6573ee6e802&pid=1-s2.0-S2590182624000092-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140948283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}