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Interactions of microplastics with heavy metals in the aquatic environment: Mechanisms and mitigation 水生环境中微塑料与重金属的相互作用:机制和缓解
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-22 DOI: 10.1016/j.hazadv.2025.100984
Atta Rasool, Jan Halfar, Kateřina Brožová, Kristina Čabanová, Jitka Chromíková, Petra Malíková, Oldřich Motyka, Eva Pertile, Silvie Drabinová, Silvie Heviánková
Microplastics (MPs) and heavy metals (HMs) are significant pollutants in aquatic ecosystems, posing substantial risks to both environmental and human health. Despite growing research interest, the quantitative understanding of MPs-HMs interactions remains limited due to methodological inconsistencies and insufficient cross-study data synthesis. This review presents a data-driven and mechanistic evaluation of these interactions, focusing on sorption and desorption mechanisms and the impact of key physicochemical parameters, including pH, salinity, temperature, and dissolved organic matter. Experimental data are analyzed to reveal trends in adsorption capacity across different polymers, particle sizes, and metal species. The review also synthesizes toxicological effects on aquatic organisms and humans and assesses recent advances in modeling and remediation approaches. Hybrid techniques integrating conventional and emerging technologies show promise for the simultaneous removal of MPs and HMs, though challenges persist for large-scale implementation. By linking quantitative trends with mechanistic insights, this review identifies critical knowledge gaps, outlines directions for future experimental validation, and supports the development of standardized protocols for environmental monitoring, risk assessment, and remediation.
微塑料(MPs)和重金属(HMs)是水生生态系统中的重要污染物,对环境和人类健康构成重大风险。尽管研究兴趣日益浓厚,但由于方法不一致和交叉研究数据合成不足,对MPs-HMs相互作用的定量理解仍然有限。本文综述了这些相互作用的数据驱动和机制评价,重点关注吸附和解吸机制以及关键物理化学参数(包括pH,盐度,温度和溶解有机质)的影响。实验数据进行分析,以揭示趋势的吸附能力跨越不同的聚合物,颗粒大小,和金属物种。该综述还综合了对水生生物和人类的毒理学影响,并评估了模拟和补救方法的最新进展。结合传统技术和新兴技术的混合技术有望同时去除MPs和HMs,尽管大规模实施仍然存在挑战。通过将定量趋势与机制见解联系起来,本综述确定了关键的知识差距,概述了未来实验验证的方向,并支持制定环境监测、风险评估和补救的标准化方案。
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引用次数: 0
In-vehicle toluene exposure affects functional connectivity of working memory retrieval networks 车内接触甲苯影响工作记忆检索网络的功能连通性
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-17 DOI: 10.1016/j.hazadv.2025.100982
Jiajing Wang , Fangfang Hao , Peiran Yu , Wenjuan Wu , Junjie Liu , Yijun Song
With the aim to investigate the impact of in-vehicle toluene exposure on working memory (WM) retrieval networks, twenty-three healthy adults underwent 4-hour exposures to toluene at concentrations of 0, 17.5, 35, or 70 ppb within a simulated vehicle. After exposure, all participants completed a WM task while cortical electroencephalography signals were recorded. The functional connectivity (FC) strengths of WM retrieval networks were compared across the four groups using direct transfer function (DTF) analysis. Results indicated that exposure to 70 ppb toluene significantly increased the FC strengths of the WM retrieval network, particularly in the frontal cortex (P < 0.05). Specifically, DTF values for FZ-T5, FZ-F3, F3-T5, F4-T6, and F7-T5 were higher at 70 ppb than those at 0 ppb (P < 0.05, P < 0.01, P < 0.001, P < 0.05, P < 0.05, respectively). The DTF values for FZ-F3 and F3-T5 at 35 ppb were higher than those at 0 ppb (P < 0.01). The DTFFZ-F3 value at 17.5 ppb was higher than that at 0 ppb (P < 0.01). The results suggest that even ppb-level, in-vehicle toluene exposure can significantly impact WM retrieval networks. The observed increase in FC strengths involved the medial prefrontal-to-left dorsolateral prefrontal cortex network, and several prefrontal-to-inferior temporal gyrus pathways. This dose-dependent enhancement of FC within critical cognitive networks presents a plausible neurophysiological mechanism for how in-vehicle toluene exposure may disrupt normal WM retrieval processes.
为了研究车内甲苯暴露对工作记忆(WM)检索网络的影响,23名健康成年人在模拟车辆中暴露于浓度为0、17.5、35或70 ppb的甲苯4小时。暴露后,所有参与者都完成了一项WM任务,同时记录了皮质脑电图信号。采用直接传递函数(DTF)分析比较四组WM检索网络的功能连通性(FC)强度。结果表明,暴露于70 ppb的甲苯显著增加了WM检索网络的FC强度,特别是在额叶皮层(P < 0.05)。其中,FZ-T5、FZ-F3、F3-T5、F4-T6和F7-T5在70 ppb时的DTF值高于0 ppb(分别为P <; 0.05、P < 0.01、P < 0.001、P < 0.05、P < 0.05)。FZ-F3和F3-T5在35 ppb下的DTF值高于0 ppb (P < 0.01)。17.5 ppb时DTFFZ-F3值高于0 ppb时(P < 0.01)。结果表明,即使是ppb水平的车内甲苯暴露也会显著影响WM检索网络。观察到的FC强度增加涉及内侧前额叶到左背外侧前额叶皮层网络,以及几个前额叶到下颞回通路。这种关键认知网络中FC的剂量依赖性增强提供了一种合理的神经生理学机制,说明车内甲苯暴露如何破坏正常的WM检索过程。
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引用次数: 0
From source to prediction: Heavy metals toxicity, health risks, detection techniques and AI- enhanced predictive models (2019–2024) 从来源到预测:重金属毒性、健康风险、检测技术和人工智能增强预测模型(2019-2024)
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-16 DOI: 10.1016/j.hazadv.2025.100981
Nafeesa Khatoon , Sartaj Ali , Zeyang Li , Mingyi Xue , Yue Han , Teng Pan , Xiaoan Zhang , Zengli Yu , Xin Zhao
Heavy metal toxicity seriously threatens the health of people, plants, and the food chain in developing countries. A review of the Science Direct, PubMed, Web of Science, Google Scholar, Springer, and Scopus databases was performed to assess the sources, exposure, toxicity mechanism, human health aspects, and detection techniques related to Cd, Cr, Mn, Ni, and Cu between 2019 and 2024. Moreover, AI-powered models particularly Random Forest (RF) for predictive analysis and Convolutional Neural Networks (CNNs) for spatial mapping to highlight significant contamination hotspot, were examined for their efficiency and reliability to identify and detect the distribution of heavy metals. The environment is frequently polluted with heavy metals as a result of improper home waste disposal, industrial and agricultural operations, and overuse of pesticides and fertilizers in developing countries. China contributed the most to heavy metals research, followed by the United States. The accumulation and exposure to heavy metals lead to potential outcomes in humans. Long-term exposure to certain heavy metals is significantly associated with increased risk of developing various cancer types such as prostate, lung, throat, breast, blood, and brain cancers. The current study found in light of the existing identification and detection techniques' pros and cons, X-ray fluorescence spectroscopy (XRF) is a promising technique to quantify and detect heavy metals owing to its rapid, on-site, and non-destructive screening method.
Based on gaps found in the literature, the current review suggests that integrating AI algorithms with nanotechnology and new biosensor platforms to accomplish high-precision, real-time environmental monitoring is an important future direction. To protect the community, longitudinal health studies, biomonitoring, and the use of green remediation technologies should be encouraged.
在发展中国家,重金属毒性严重威胁着人、植物和食物链的健康。对Science Direct、PubMed、Web of Science、谷歌Scholar、施普林格和Scopus数据库进行了回顾,以评估2019年至2024年间与Cd、Cr、Mn、Ni和Cu相关的来源、暴露、毒性机制、人类健康方面和检测技术。此外,人工智能驱动的模型,特别是用于预测分析的随机森林(RF)和用于空间映射的卷积神经网络(cnn),以突出重要的污染热点,研究了它们识别和检测重金属分布的效率和可靠性。在发展中国家,由于家庭废物处理不当、工业和农业作业以及过度使用杀虫剂和化肥,环境经常受到重金属污染。中国对重金属研究的贡献最大,其次是美国。重金属的积累和暴露会对人类造成潜在的后果。长期接触某些重金属会显著增加患各种癌症的风险,如前列腺癌、肺癌、喉癌、乳腺癌、血癌和脑癌。目前的研究发现,鉴于现有鉴定和检测技术的优缺点,x射线荧光光谱(XRF)以其快速、现场、无损的筛选方法,是一种很有前途的重金属定量和检测技术。基于文献中发现的空白,目前的综述表明,将人工智能算法与纳米技术和新的生物传感器平台相结合,以实现高精度、实时的环境监测是一个重要的未来方向。为保护社区,应鼓励进行纵向健康研究、生物监测和使用绿色修复技术。
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引用次数: 0
Anthropogenic footprint and ecological risk assessment of organochlorine pesticides and polychlorinated biphenyls in sediments from Lake Victoria, East Africa 东非维多利亚湖沉积物中有机氯农药和多氯联苯的人为足迹及生态风险评价
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-15 DOI: 10.1016/j.hazadv.2025.100979
Afuwa Kagoya , Kenneth Arinaitwe , Silver Odongo , Douglas Sifuna , Henry Matovu , Julius Matsiko , Godfrey Muhwezi , Ivan Špánik , Charles Drago Kato , Mika Sillanpaä , Patrick Ssebugere
Lake Victoria, the world’s second-largest freshwater lake, continues to face pressure from anthropogenic activities in its catchment area, releasing pollutants, which are ultimately trapped in the sediment core, thereby posing threats to aquatic organisms. This study quantified thirteen organochlorine pesticides (OCPs) and ten polychlorinated biphenyls (PCBs) in sediments from the Uganda, Kenya, and Tanzania sides of Lake Victoria using soxhlet method, fractionation column and GC–MS/MS analysis. Total (∑13) OCPs levels were up to 412, 148, and 522 µg kg-1 dry weight (d.w), and 12.1, 8.69 and 9.87 µg kg-1 dw for total (∑10) PCBs for sediments from Uganda, Kenya, and Tanzania, respectively. Diagnostic ratios suggested past and ongoing use of OCPs while principal component analysis confirmed that OCP profiles were mainly due to their application in controlling pests in agriculture and public health programs, and PCB congeners were largely due to volatilization, degradation of higher PCBs into lighter PCBs, improper waste disposal of old transformers, hydraulic fluids, plasticizers, and capacitors. Ecological risk assessment highlighted that the PCB levels in sediments were below threshold effect and probable effect levels, but p,p′-DDD, and lindane were likely to pose adverse effects to sediment-dwelling organisms in Lake Victoria. These results imply persistent pollutant loads in Lake Victoria, and consequently, a need for its enhanced management.
维多利亚湖是世界第二大淡水湖,其集水区持续面临着人类活动的压力,释放出的污染物最终被困在沉积物核心,从而对水生生物构成威胁。采用索氏法、分馏柱法和GC-MS /MS法对维多利亚湖乌干达、肯尼亚和坦桑尼亚沿岸沉积物中的13种有机氯农药(OCPs)和10种多氯联苯(PCBs)进行了定量分析。乌干达、肯尼亚和坦桑尼亚沉积物的总(∑13)PCBs含量分别为412、148和522µg kg-1干重(d.w),总(∑10)PCBs含量分别为12.1、8.69和9.87µg kg-1 dw。诊断比率表明过去和正在使用OCP,而主成分分析证实OCP主要是由于其在农业和公共卫生项目中控制害虫的应用,而PCB同源物主要是由于挥发,高含量多氯联苯降解为较轻的多氯联苯,旧变压器,液压油,增塑剂和电容器的不当废物处理。生态风险评估结果表明,沉积物中多氯联苯含量低于阈值效应和可能效应水平,但p、p ' -DDD和林丹可能对维多利亚湖沉积物生物产生不利影响。这些结果表明维多利亚湖的污染物负荷持续存在,因此需要加强对其的管理。
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引用次数: 0
Long-term source apportionment and assessment of metals in lake sediments contaminated by mining and smelting in South Korea 韩国采矿和冶炼污染湖泊沉积物中金属的长期来源分析与评价
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-15 DOI: 10.1016/j.hazadv.2025.100980
Dong-Jin Joe , Man-Sik Choi , Yun-ho Song
Understanding the long-term evolution and sources of metal contamination in lacustrine environments is essential for assessing ecological risks and informing remediation. This study reconstructs the historical and spatial distribution of heavy metals in sediments of Andong Lake, an artificial reservoir in South Korea impacted by legacy mining and smelting activities. Eight sediment cores were collected along the lake’s main axis and analyzed for geochemical properties and concentrations of cadmium (Cd), zinc (Zn), copper (Cu), lead (Pb), arsenic (As), nickel (Ni), manganese (Mn), cobalt (Co), and lithium (Li).
Sediment chronology was constrained using 210Pb dating and stratigraphic boundaries corresponding to dam construction in 1976. Vertical metal profiles revealed two contamination phases: (1) substantial enrichment of Cd, Zn, Cu, Pb, Ni, Mn, and Co during 1976–1995, linked to discharges from upstream Pb–Zn mines (mining-derived materials, MDMs), and (2) renewed increases in Cd and Zn since 2005, associated with emissions from a Zn smelter (smelting-derived materials, SDMs).
By integrating Li-normalized metal ratios and historical production data, the relative contributions of MDMs and SDMs to baseline sediments (1995–2005) were quantified. MDMs contributed up to 42.6 % of Cd and 50.0 % of Zn during the early post-dam phase (1976–1995), while SDMs accounted for approximately 42.8 % of Cd and 29.7 % of Zn in recent decades (2005–2020).
This study establishes a transferable framework that integrates sediment chronology, normalized geochemical indicators, and industrial production records to trace long-term metal contamination in large artificial lakes—providing new insights for pollution source apportionment and reservoir management.
了解湖泊环境中金属污染的长期演变和来源对评估生态风险和提供修复信息至关重要。本研究重建了受采矿和冶炼活动影响的韩国安东湖人工水库沉积物中重金属的历史和空间分布。研究人员沿湖泊主轴收集了8个沉积物岩心,分析了镉(Cd)、锌(Zn)、铜(Cu)、铅(Pb)、砷(As)、镍(Ni)、锰(Mn)、钴(Co)和锂(Li)的地球化学性质和浓度。采用210Pb定年法和1976年大坝建设对应的地层界线对沉积物年代学进行了约束。垂直金属剖面揭示了两个污染阶段:(1)1976-1995年期间Cd、Zn、Cu、Pb、Ni、Mn和Co的大量富集,与上游铅锌矿(采矿衍生材料,MDMs)的排放有关;(2)自2005年以来Cd和Zn的再次增加,与锌冶炼厂(冶炼衍生材料,SDMs)的排放有关。通过整合锂标准化金属比例和历史生产数据,量化了MDMs和SDMs对基线沉积物的相对贡献(1995-2005)。在坝后早期(1976-1995年),MDMs贡献了42.6%的Cd和50.0%的Zn,而近几十年(2005-2020年)SDMs贡献了42.8%的Cd和29.7%的Zn。本研究建立了一个可转移的框架,将沉积物年代学、标准化地球化学指标和工业生产记录结合起来,追踪大型人工湖的长期金属污染,为污染源分配和水库管理提供了新的见解。
{"title":"Long-term source apportionment and assessment of metals in lake sediments contaminated by mining and smelting in South Korea","authors":"Dong-Jin Joe ,&nbsp;Man-Sik Choi ,&nbsp;Yun-ho Song","doi":"10.1016/j.hazadv.2025.100980","DOIUrl":"10.1016/j.hazadv.2025.100980","url":null,"abstract":"<div><div>Understanding the long-term evolution and sources of metal contamination in lacustrine environments is essential for assessing ecological risks and informing remediation. This study reconstructs the historical and spatial distribution of heavy metals in sediments of Andong Lake, an artificial reservoir in South Korea impacted by legacy mining and smelting activities. Eight sediment cores were collected along the lake’s main axis and analyzed for geochemical properties and concentrations of cadmium (Cd), zinc (Zn), copper (Cu), lead (Pb), arsenic (As), nickel (Ni), manganese (Mn), cobalt (Co), and lithium (Li).</div><div>Sediment chronology was constrained using <sup>210</sup>Pb dating and stratigraphic boundaries corresponding to dam construction in 1976. Vertical metal profiles revealed two contamination phases: (1) substantial enrichment of Cd, Zn, Cu, Pb, Ni, Mn, and Co during 1976–1995, linked to discharges from upstream Pb–Zn mines (mining-derived materials, MDMs), and (2) renewed increases in Cd and Zn since 2005, associated with emissions from a Zn smelter (smelting-derived materials, SDMs).</div><div>By integrating Li-normalized metal ratios and historical production data, the relative contributions of MDMs and SDMs to baseline sediments (1995–2005) were quantified. MDMs contributed up to 42.6 % of Cd and 50.0 % of Zn during the early post-dam phase (1976–1995), while SDMs accounted for approximately 42.8 % of Cd and 29.7 % of Zn in recent decades (2005–2020).</div><div>This study establishes a transferable framework that integrates sediment chronology, normalized geochemical indicators, and industrial production records to trace long-term metal contamination in large artificial lakes—providing new insights for pollution source apportionment and reservoir management.</div></div>","PeriodicalId":73763,"journal":{"name":"Journal of hazardous materials advances","volume":"21 ","pages":"Article 100980"},"PeriodicalIF":7.7,"publicationDate":"2025-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145790576","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}
引用次数: 0
Genotypic variation in physiological and molecular responses underpins differential germanium tolerance in rice (Oryza sativa L.) 水稻(Oryza sativa L.)生理和分子反应的基因型变异支持锗的差异耐受
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-14 DOI: 10.1016/j.hazadv.2025.100978
Saireen Ahsen , Shuxin Tu , Muhammad Ahmad Javeed , Khurram Shehzad , Muhammad Baqir Hussain
Germanium (Ge) exhibits dual effects in plants, ranging from beneficial to toxic, depending on its concentration and the plant genotype. A germination-based screening of 18 diverse rice varieties identified TXY2115 and CLY669 as tolerant, and ZXY1205 and ZZY8 as sensitive to Ge stress. This study elucidates the physiological and molecular mechanisms underpinning this differential tolerance under escalating Ge stress (0–40 mg l-1). The tolerant genotypes effectively mitigated Ge toxicity, sustaining superior growth, higher biomass, and preserving photosynthetic function, evidenced by 18–25 % higher stomatal conductance. This superior photosynthetic function, despite similar percent reductions in total chlorophyll content (56 % in tolerant vs. 54 % in sensitive varieties at 40 mg l-1 Ge), is explained by two key traits: (1) tolerant varieties retained a higher chlorophyll a/b ratio (1.8 ± 0.1 vs. 1.4 ± 0.1 in sensitive genotypes), preserving photosystem II (PSII) stability, and (2) stronger coupling between stomatal conductance (Gs) and net photosynthetic rate (Pn) (r = 0.83, p < 0.01), as observed in arsenic-tolerant rice. The cornerstone of their tolerance was a preemptive and highly coordinated antioxidant defense system. This was characterized by a significantly enhanced capacity to activate antioxidant enzymes (11–40 % higher Superoxide Dismutase,(SOD) and Catalase (CAT) activity), boost key metabolites like glutathione (33 % higher root GSH), and strongly upregulate the expression of core antioxidant genes (OsSOD1 and OsCAT1). This robust multi-level response effectively curtailed oxidative damage, resulting in 37–53 % lower ROS and 45–58 % lower Malondialdehyde (MDA) levels than the sensitive varieties at high Ge concentrations. This research provides a critical framework for assessing Ge’s role in agriculture, its mitigation, and identifies specific targets for breeding crops resilient to Ge stress or suitable for Ge biofortification.
锗(Ge)在植物中表现出双重作用,根据其浓度和植物基因型的不同,既有有益作用,也有毒性作用。通过对18个不同水稻品种的发芽筛选,发现TXY2115和CLY669对Ge胁迫具有耐受性,而ZXY1205和ZZY8对Ge胁迫敏感。本研究阐明了在不断升高的Ge胁迫(0-40 mg -1)下这种差异耐受性的生理和分子机制。耐受性基因型有效减轻了Ge毒性,维持了较好的生长,较高的生物量,并保持了光合功能,气孔导度提高了18 - 25%。尽管总叶绿素含量在40 mg l-1 Ge下降低了相似的百分比(耐受性品种为56%,敏感性品种为54%),但这种优越的光合功能可以用两个关键性状来解释:(1)耐砷品种保持了较高的叶绿素a/b比(敏感基因型为1.8±0.1比1.4±0.1),保持了光系统II (PSII)的稳定性;(2)气孔导度(Gs)与净光合速率(Pn)之间的耦合更强(r = 0.83, p < 0.01),在耐砷水稻中观察到。他们的耐受性的基石是一个先发制人和高度协调的抗氧化防御系统。其特点是显著增强了抗氧化酶的激活能力(超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性提高了11 - 40%),提高了关键代谢物如谷胱甘肽(根GSH提高了33%),并强烈上调了核心抗氧化基因(OsSOD1和OsCAT1)的表达。这种强大的多层次反应有效地减少了氧化损伤,导致ROS水平比高Ge浓度下的敏感品种低37 - 53%,丙二醛(MDA)水平低45 - 58%。这项研究为评估Ge在农业中的作用及其缓解提供了一个关键框架,并确定了培育抗Ge胁迫或适合Ge生物强化的作物的具体目标。
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引用次数: 0
A review of in-situ technologies for enhancement of the removal of pharmaceuticals and personal care products (PPCPs) and mitigation of membrane fouling in membrane bioreactors 膜生物反应器中增强药物和个人护理产品(PPCPs)去除和缓解膜污染的原位技术综述
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-13 DOI: 10.1016/j.hazadv.2025.100976
Tanissorn Buakaew , Chavalit Ratanatamskul
The widespread presence of pharmaceuticals and personal care products (PPCPs) in wastewater, along with the persistent issue of membrane fouling, has intensified the demand for enhanced membrane bioreactor (MBR) performance. This review critically evaluates in-situ technologies designed to improve PPCP removal while reducing membrane fouling within MBR systems. Strategies include MBR configuration modifications, optimization of operational parameters, microbial manipulation approaches, and the dosing of exogenous physicochemical additives (e.g., activated carbon, coagulants, iron-based compounds). Furthermore, advanced techniques such as electrically assisted MBR, advanced oxidation process (AOP) assisted MBRs, and the development of novel membrane materials and surface coatings are discussed for their dual functionalities in pollutant removal and fouling resistance. Each approach presents specific advantages and limitations in terms of removal efficiency, operational complexity, cost, and environmental impact. This review emphasizes the importance of integrating multiple strategies in a synergistic manner, supported by intelligent monitoring, automation, and sustainability principles. Future advancements should focus on hybrid systems that combine biological, chemical, and physical enhancements with cost-effective and energy-efficient operation, paving the way for next-generation MBR technologies capable of delivering high-performance, low-impact wastewater treatment.
废水中广泛存在的药品和个人护理产品(PPCPs),以及持续存在的膜污染问题,加剧了对增强膜生物反应器(MBR)性能的需求。这篇综述批判性地评估了原位技术,旨在提高PPCP去除,同时减少MBR系统中的膜污染。策略包括MBR配置修改、操作参数优化、微生物操作方法和外源物理化学添加剂(如活性炭、混凝剂、铁基化合物)的剂量。此外,还讨论了电辅助MBR、高级氧化工艺(AOP)辅助MBR等先进技术,以及新型膜材料和表面涂层的发展,因为它们具有去除污染物和抗污染的双重功能。每种方法在去除效率、操作复杂性、成本和环境影响方面都有各自的优点和局限性。这篇综述强调了在智能监测、自动化和可持续性原则的支持下,以协同方式整合多种战略的重要性。未来的发展应该集中在将生物、化学和物理增强与成本效益和节能操作相结合的混合系统上,为能够提供高性能、低影响废水处理的下一代MBR技术铺平道路。
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引用次数: 0
A design of experiments approach to arsenic retention: Interactions between sediment properties and water chemistry 砷保留的实验方法设计:沉积物性质与水化学之间的相互作用
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-13 DOI: 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.
地下水中砷(As)的迁移受沉积物-水界面的动态相互作用控制,其中矿物反应性和水化学起关键作用。在Como含水层(意大利北部),As的垂直分布不均匀:浅层仍低于世卫组织10微克/升的限值,而较深区域的浓度高达250微克/升。尽管这种可变性有很好的文献记载,但潜在的机制仍然只是部分地被理解。为了解决这一空白,我们在全因子实验设计中对浅层和深层含水层沉积物进行了批量实验,对比了它们的组成,系统地改变了pH值,电导率和溶解有机碳。结果显示了非线性吸附响应和沉积物特异性行为。浅层沉积物表现出更强、更稳定的As滞留,具有较高的Fe-、Al-和Mn-(氢)氧化物含量和更大的阳离子交换能力。而深层沉积物在酸性、doc富集和高导电性条件下的吸附能力较弱且变化较大。响应面模型证实,沉积物组成决定了砷截留能力,而水化学调节其效率。这种综合方法将实验室吸附模式与现场尺度的砷分布联系起来,为科莫含水层观测到的垂直非均质性提供了机制解释,并支持地下水脆弱性的预测评估。
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引用次数: 0
Understanding the co-occurrence patterns and geochemical evolution pathways of complex geogenic groundwater contamination: A case study of the Ganjiang River Delta 复杂地源性地下水污染共生模式与地球化学演化路径——以赣江三角洲为例
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-13 DOI: 10.1016/j.hazadv.2025.100973
Jingwen Zhang , Yongming Wu , Zhangjun Liu , Yajun Liu , Mi Deng , Xiangming Liu , Rongfu Li , Zeyong Chi
The study investigates the complex mixture of geogenic contaminants (GCs) in the groundwater of the Ganjiang River Delta via hydrochemical, isotopic, and multivariate statistical methods, focusing on their co-occurrence patterns and evolutionary mechanisms. Fe, Mn, As, NH4+-N, S(II), I, and P were identified as the main GCs, with strong correlations observed between Mn and I, whereas Fe, P, As, and NH4+-N were closely associated. Under weakly reducing conditions, the reductive dissolution of I-bearing Mn(IV)-oxides caused the co-occurrence of I and Mn. As the reducing environment intensifies, the evolution of GCs diverged into two geochemical pathways based on organic matter (OM) availability. In organic-rich areas, the reductive dissolution of As-bearing Fe(III)-oxides coupled with As(V) reduction led to moderate concentrations of Fe and As. Subsequently, the consumption of labile OM triggered Mn(II)-dependent autotrophic denitrification (AuDen), which lowered Mn and I concentrations in a strongly reducing environment. In contrast, in organic-poor areas, the reductive dissolution of Fe(III)-oxides induced by iron ammonium oxidation, along with secondary As(V) adsorption, caused the decoupling of As and Fe. This was followed by Fe(II)-dependent AuDen, which decreased Fe and related GCs concentrations in a strongly reducing environment. Under deeply reducing conditions, both pathways were dominated by the crystalline Fe(III)-oxides-mediated degradation of refractory OM, leading to the co-release of GCs. This study highlights the controlling roles of redox conditions and OM in the formation and evolution of complex geogenic contaminated groundwater (CGCG). Our results also suggest that enhancing AuDen may be a promising in-situ remediation strategy for CGCG.
运用水化学、同位素和多元统计等方法,研究了赣江三角洲地下水中复杂的地质污染物混合物,重点探讨了它们的共生模式和演化机制。主要gc为Fe、Mn、As、NH4+-N、S(II)、I和P,其中Mn和I相关性较强,Fe、P、As和NH4+-N相关性较强。在弱还原条件下,含I Mn(IV)氧化物的还原性溶解导致I和Mn共存。随着还原环境的加剧,gc的演化以有机质(OM)有效性为基础,分化为两条地球化学路径。在富有机质地区,含As的Fe(III)氧化物的还原性溶解加上As(V)的还原导致了中等浓度的Fe和As。随后,不稳定OM的消耗触发了Mn(II)依赖性自养反硝化(AuDen),在强还原环境中降低了Mn和I的浓度。相比之下,在有机贫乏地区,铁铵氧化诱导Fe(III)-氧化物的还原性溶解以及As(V)的二次吸附导致了As和Fe的解耦。其次是Fe(II)依赖性AuDen,在强还原环境中降低了Fe和相关GCs浓度。在深度还原条件下,这两种途径都以晶体Fe(III)氧化物介导的难降解OM降解为主,导致gc的共释放。本研究强调了氧化还原条件和有机质在复杂地源污染地下水(CGCG)形成和演化中的控制作用。我们的研究结果还表明,增强AuDen可能是一种有前途的原位修复CGCG的策略。
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引用次数: 0
Gasification-flameless and N₂O-assisted combustion for ultra-low PCDD/F emissions from chlorine-rich solid recovered fuel 气化无火焰和N₂辅助燃烧,用于富氯固体回收燃料的超低PCDD/F排放
IF 7.7 Q2 ENGINEERING, ENVIRONMENTAL Pub Date : 2025-12-12 DOI: 10.1016/j.hazadv.2025.100971
Sheng-Lun Lin , Wei Tang , Yu-Lun Hsieh , Jhong-Lin Wu
Chlorine‑rich solid recovered fuel (Cl‑SRF) poses persistent risks of polychlorinated dibenzo‑p‑dioxin and dibenzofuran (PCDD/F) formation and a high operational burden on air‑pollution control systems (APCS). Meanwhile, the valorization of nitrous oxide (N₂O) in waste‑to‑energy systems remains underexplored, creating a gap between emission control needs and oxidant utilization. This study pioneers a "waste-treats-waste" strategy by integrating gasification-flameless combustion (GFCM) with N₂O-assisted combustion (NACM) to simultaneously suppress PCDD/Fs and utilize residual N₂O. Pilot‑scale tests with chlorine‑rich SRF (1.58 wt%) show that NACM achieves a 95.7 % reduction in total PCDD/F mass concentration (to 15.3 ng/Nm³) and lowers stack toxicity to 0.044 ng WHO‑TEQ/Nm³, well below stringent limits. GFCM reduced conventional CO and NOx emissions by 36 % and 66 %, respectively, versus diffusion combustion (DCM), while NACM maintains NOx 52 % below DCM and improves thermal homogeneity in the primary chamber. Perfectly stirred reactor kinetic modeling indicates that reactive oxygen radicals from N₂O decomposition inhibit chlorinated precursors with a negligible NOx penalty. Ultimately, this approach enables the safe valorization of high-chlorine waste fuels, demonstrating a robust pathway for a circular economy by converting problematic waste streams into sustainable energy.
富氯固体回收燃料(Cl - SRF)持续存在形成多氯二苯并对二恶英和二苯并呋喃(PCDD/F)的风险,并给空气污染控制系统(APCS)带来沉重的运行负担。与此同时,一氧化二氮(N₂O)在废物转化为能源系统中的价值仍未得到充分探索,这在排放控制需求和氧化剂利用之间造成了差距。本研究开创了一种“废物-处理-废物”策略,通过将气化-无火焰燃烧(GFCM)与N₂辅助燃烧(ncm)相结合,同时抑制PCDD/Fs并利用剩余N₂O。富氯SRF (1.58 wt%)的中试规模试验表明,ncm可将PCDD/F总质量浓度降低95.7%(降至15.3 ng/Nm³),并将堆叠毒性降低至0.044 ng WHO‑TEQ/Nm³,远低于严格的限值。与扩散燃烧(DCM)相比,GFCM将传统的CO和NOx排放量分别降低了36%和66%,而ncm将NOx排放量保持在比DCM低52%的水平,并改善了主燃烧室的热均匀性。完全搅拌反应器动力学模型表明,N₂O分解产生的活性氧自由基对氯化前驱体的抑制作用可以忽略不计。最终,这种方法能够使高氯废物燃料安全增值,通过将有问题的废物流转化为可持续能源,展示了循环经济的有力途径。
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引用次数: 0
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Journal of hazardous materials advances
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