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The Synergy of Adsorption and Advanced Oxidation for Enhanced Microplastic Abatement in Water 吸附与深度氧化协同强化水中微塑料去除
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-09-30 DOI: 10.1007/s40726-026-00430-9
Yingwei Qin, Xiaoyan Wang, Cuizhu Sun, Hao Zheng, Xianxiang Luo, Lingyun Chen, Fengmin Li

Purpose of Review

Microplastic (MP) pollution in water environments threatens ecological safety and human health. The small size, hydrophobicity, and large surface area of MPs facilitate ingestion by marine organisms and their role as vectors for co‑occurring contaminants, thereby amplifying ecological and health risks. Existing wastewater treatment facilities can remove over 90% of large MPs (> 50 μm), but the removal and degradation of fine MPs and nanoplastics remain difficult because of their high mobility, low settling rates, and polymer backbones. Unlike prior reviews focused on standalone treatments or dissolved pollutants, this review addresses adsorption-advanced oxidation process (AOP) synergistic technologies for particulate MP abatement, emphasizing the interfacial coupling between MP enrichment and in situ oxidative degradation in adsorption-photocatalysis, adsorption-Fenton, and adsorption-electrochemical oxidation systems.

Recent Findings

Adsorption offers high enrichment efficiency, while AOPs (e.g., photocatalysis, Fenton, persulfate oxidation, ozonation, and electrochemical oxidation) generate strong reactive species. However, each standalone method has inherent limitations. Adsorption merely transfers MPs to another phase, leading to secondary pollution, whereas AOPs are constrained by poor mass transfer and low radical utilization at low MP concentrations. Integrated adsorption‑AOP synergistic systems leverage a targeted enrichment-in situ degradation mechanism to increase local MP concentration, shorten mass‑transfer paths, and achieve concurrent enrichment and oxidation. Key adsorption-catalysis interfaces include carbon‑based materials, metal-organic frameworks (MOFs), covalent organic frameworks (COFs), chitin‑based materials, and conductive electrodes, which facilitate MP capture, interfacial activation, and reactive oxygen species (ROS) utilization.

Summary

Adsorption‑AOPs synergistic technologies outperform standalone approaches by enabling targeted enrichment and in situ MP degradation, thereby overcoming the low removal efficiency for small MPs. This review clarifies how interfacial enrichment, mass-transfer modulation, and localized ROS utilization underpin the synergy of adsorption-AOPs. Future work should prioritize long‑term stability, performance under real‑water matrix conditions, secondary‑risk assessment, toxicity reduction, and cost evaluation to promote standardized and practical MP pollution control in water environments.

Graphical Abstract

水环境中的微塑料污染威胁着生态安全和人类健康。MPs的小尺寸、疏水性和大表面积有利于海洋生物的摄入,并可作为同时发生的污染物的载体,从而扩大生态和健康风险。现有的废水处理设施可以去除90%以上的大型MPs (> 50 μm),但由于其高迁移率、低沉降率和聚合物骨架,精细MPs和纳米塑料的去除和降解仍然很困难。不同于以往的文献关注于独立处理或溶解污染物,本综述探讨了吸附-高级氧化过程(AOP)协同技术用于颗粒MP减排,强调了吸附-光催化、吸附- fenton和吸附-电化学氧化系统中MP富集与原位氧化降解之间的界面耦合。吸附具有较高的富集效率,而AOPs(如光催化、Fenton、过硫酸盐氧化、臭氧氧化和电化学氧化)产生较强的活性物质。然而,每种独立的方法都有其固有的局限性。吸附只是将MPs转移到另一相,导致二次污染,而AOPs在低MP浓度下受到传质差和自由基利用率低的限制。集成的吸附- AOP协同系统利用靶向富集-原位降解机制来增加局部MP浓度,缩短传质路径,并实现同步富集和氧化。关键的吸附催化界面包括碳基材料、金属有机框架(MOFs)、共价有机框架(COFs)、几丁质基材料和导电电极,它们有助于MP捕获、界面激活和活性氧(ROS)的利用。吸附- AOPs协同技术优于独立方法,实现了靶向富集和原位MP降解,从而克服了小MP的低去除效率。这篇综述阐明了界面富集、传质调制和局部ROS利用如何支撑吸附- aops的协同作用。未来的工作应优先考虑长期稳定性、真实水基质条件下的性能、二次风险评估、毒性降低和成本评估,以促进水环境中标准化和实用的MP污染控制。图形抽象
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引用次数: 0
A Perspective Review of Per- and Polyfluoralkyl Substances (PFAS) as Emerging Contaminants in Environment: Removal, Transport, Metabolic Process and Future Direction 全氟和多氟烷基物质(PFAS)作为环境中新出现的污染物:去除、运输、代谢过程和未来发展方向
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-09-07 DOI: 10.1007/s40726-026-00428-3
Anisa Ratnasari

Purpose of review

PFAS are commonly used in industrial process. Nonetheless, they are persistent in environment leading to a significant threat to organisms and human health. This perspective review traces the occurrence, extraction including separation and analysis, and removal methods of PFAS in environment to reveal their effectiveness, mechanism, and scalable, also enabling their advancement.

Recent findings

The highest PFAS accumulation was found, including PFDS (62.56 ng/g), PFOS (40237 ng/mg), 6:2 FTOH (500 pg/m3), and PFPHpA (43.20 ng/L) in sediment, soil, atmosphere, and surface water. They can accumulate in liver, intestine, muscle, spleen, renal, lung, cytoplasm, plasma, hepatocytes, and placenta. In environment, transport takes place via hydrophobic, electrostatic, ligand exchange, and hydrogen bonds. PFAS contaminate organisms via passive diffusion, active transport, transformation, accumulation, and excretion.

Summary

Integrated technique is the promising removal strategy since have better performance compared to stand alone technique, whilst temperature, humidity, carbon content, mass ratio, and time transport influence PFAS removals. In the future, these findings will guide strategies to prevent PFAS contamination.

pfas在工业生产过程中被广泛使用。然而,它们在环境中持续存在,对生物和人类健康构成重大威胁。本文综述了PFAS在环境中的发生、提取、分离、分析和去除方法,揭示了PFAS的有效性、机理和可扩展性,并为PFAS的发展奠定了基础。在沉积物、土壤、大气和地表水中,PFDS (62.56 ng/g)、PFOS (40237 ng/mg)、6:2 FTOH (500 pg/m3)和PFPHpA (43.20 ng/L)的累积量最高。它们可积聚在肝、肠、肌肉、脾、肾、肺、细胞质、血浆、肝细胞和胎盘中。在环境中,转运通过疏水、静电、配体交换和氢键进行。PFAS通过被动扩散、主动运输、转化、积累和排泄等途径污染生物体。综合技术是一种很有前途的去除策略,因为与独立技术相比,综合技术具有更好的性能,而温度、湿度、碳含量、质量比和时间输运会影响PFAS的去除。在未来,这些发现将指导预防PFAS污染的策略。
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引用次数: 0
Compound Climate Extremes: Interactions, Emerging Urban Stressors, and Impacts on Water Quality 复合极端气候:相互作用、新出现的城市压力源和对水质的影响
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-08-31 DOI: 10.1007/s40726-026-00427-4
Aanchal Kumari, Durga Prasad Panday, Kanchan Deoli Bahukhandi, Aldo I. Ramirez, Manish Kumar

Purpose of Review

This review examines the interactions and cascading impacts of compound climate extremes, such as concurrent droughts, heatwaves, and floods, under climate change. It highlights their growing yet often overlooked threats to water quality, food security, and ecosystem resilience, and emphasizes their systemic implications for coupled human–environment systems.

Recent Findings

Recent literature reveals that compound extremes such as concurrent droughts, floods, and heatwaves generate amplified and disproportionate impacts due to their interdependent dynamics. Urbanization intensifies these effects by disrupting hydrological processes and enhancing thermal retention through mechanisms like the urban heat island effect. Despite growing recognition of their complexity, most predictive models remain limited by inadequate feedback integration, insufficient spatiotemporal resolution, and uneven regional adaptation capacities. This review highlights mounting evidence that compound extremes significantly degrade water quality by mobilizing both geogenic and emerging contaminants such as heavy metals, nutrients, pharmaceuticals, and microplastics under shifting flow, temperature, and redox conditions. While quantile-based thresholds and hazard overlays are commonly used for characterizing these events, gaps remain in linking compound hazard typologies with contaminant pathways and water system responses across diverse climatic and infrastructural contexts.

Summary

This review synthesizes global literature on compound climate extremes to identify event patterns, vulnerabilities, and modeling gaps. It underscores the need for integrated planning, early warning systems, and adaptive governance to manage escalating multi-hazard risks. Particular focus is placed on emerging contaminant mobilization, urban stressors, and scalable resilience strategies, offering actionable insights for climate-informed decision-making.

本文综述了气候变化背景下干旱、热浪和洪水等复合极端气候的相互作用和级联影响。它强调了它们对水质、粮食安全和生态系统恢复力日益增长但往往被忽视的威胁,并强调了它们对人类-环境耦合系统的系统性影响。最近的发现最近的文献表明,复合极端事件,如并发的干旱、洪水和热浪,由于它们相互依存的动态,会产生放大和不成比例的影响。城市化通过破坏水文过程和通过城市热岛效应等机制增强热保持,从而加剧了这些影响。尽管人们越来越认识到其复杂性,但大多数预测模型仍然受到反馈整合不足、时空分辨率不足和区域适应能力不均衡的限制。这篇综述强调了越来越多的证据表明,复合极端条件通过在流动、温度和氧化还原条件下调动地质和新出现的污染物,如重金属、营养物质、药物和微塑料,显著降低了水质。虽然基于分位数的阈值和危害叠加通常用于描述这些事件的特征,但在将复合危害类型与不同气候和基础设施背景下的污染物途径和水系统响应联系起来方面仍然存在差距。本综述综合了全球关于复合极端气候的文献,以确定事件模式、脆弱性和建模差距。它强调需要综合规划、早期预警系统和适应性治理来管理不断升级的多重灾害风险。特别关注新出现的污染物动员、城市压力源和可扩展的弹性战略,为气候知情决策提供可操作的见解。
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引用次数: 0
Spatiotemporal Distribution Patterns and Risk Assessment of Non-oxidizing Antimicrobials (NOAMs) in Environments: A Global Perspective 非氧化性抗微生物药物(NOAMs)在环境中的时空分布模式和风险评估:一个全球视角
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-07-30 DOI: 10.1007/s40726-026-00426-5
Jia-Qi Song, Shu-Chang Pang, Dao-Qian Chen, Nan Huang

Purpose of review

Non-oxidizing antimicrobials (NOAMs) are extensively used in domestic and industrial applications due to their excellent chemical stability and broad-spectrum antimicrobial efficacy. These compounds are frequently detected in surface waters globally, raising significant ecological concerns. This review aims to clarify the spatiotemporal distribution patterns of NOAMs in global surface waters and the key factors influencing their occurrence. Furthermore, it evaluates the toxicity, mobility, and biodegradability of NOAMs and their transformation products.

Recent findings

Global monitoring indicates that the concentrations of NOAMs in surface waters vary significantly across regions. While regulatory measures correlate with reduced loads in wastewater, pandemic-driven use, non-point sources, and sediment release also influence surface water levels. Carbendazim poses high ecological risk; azoles, triclosan, and isothiazolinones show moderate risk; quaternary ammonium compounds (QACs) are low risk. Most NOAMs form more mobile transformation products during photolysis or oxidation. Although isothiazolinone and climbazole products are generally less toxic, nearly 50% of fluconazole’s products exceed parental toxicity. Biodegradability varies: isothiazolinone products degrade readily, QAC products persist longer than the parent compound, and azole-related products often endure for months.

Summary

Ecological risk assessments of NOAMs must extend beyond parent compounds to fully account for the toxicity, mobility, and biodegradability of their transformation products. Future chemical management should adopt a life-cycle risk assessment framework that incorporates the environmental fate of transformation products into monitoring programs. Although many NOAMs are functionally interchangeable as antimicrobials, they differ substantially in ecological risk and treatability. Therefore, regulatory strategies should shift from end-of-pipe treatment toward source-oriented design, prioritizing low-toxicity, readily treatable green alternatives.

非氧化性抗菌剂(NOAMs)因其优异的化学稳定性和广谱抗菌效果而广泛应用于生活和工业领域。这些化合物经常在全球地表水中被检测到,引起了重大的生态问题。本文旨在阐明全球地表水NOAMs的时空分布格局及其发生的关键影响因素。此外,它还评估了NOAMs及其转化产物的毒性、移动性和生物降解性。最近的发现全球监测表明,不同地区地表水中NOAMs的浓度差异很大。虽然管制措施与减少废水中的负荷有关,但大流行导致的使用、非点源和沉积物释放也会影响地表水的水位。多菌灵具有较高的生态风险;唑类、三氯生和异噻唑啉类具有中等风险;季铵盐类化合物(QACs)风险较低。大多数NOAMs在光解或氧化过程中形成更多的可移动转化产物。虽然异噻唑啉酮和克里巴唑产品一般毒性较低,但近50%的氟康唑产品超过亲本毒性。生物降解性各不相同:异噻唑啉酮产品易于降解,QAC产品比母体化合物持续时间更长,而唑类产品通常持续数月。NOAMs的生态风险评估必须超越母体化合物,以充分考虑其转化产物的毒性、移动性和生物降解性。未来的化学品管理应采用生命周期风险评估框架,将转化产品的环境命运纳入监测程序。虽然许多非甾体抗微生物药物在功能上可与抗菌素互换,但它们在生态风险和可治疗性方面存在很大差异。因此,监管策略应从管道末端处理转向以源头为导向的设计,优先考虑低毒性、易于处理的绿色替代品。
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引用次数: 0
Heavy Metals and Metalloids in Food, Water, and Soil: Propagation Pathways Diagnostic Analytical Technique Practices 食物、水和土壤中的重金属和类金属:传播途径诊断分析技术实践
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-07-23 DOI: 10.1007/s40726-026-00421-w
Yetzin Rodríguez Mejía, Josue Abraham Lara Zavala, Naveen Kumar Reddy Bogireddy, Victor Barba

Purpose of Review

This review looks at how the chemical forms, movement, and availability of metal and metalloid contaminants affect food safety and public health. It brings together recent developments in detecting these contaminants in soil, water, and food, and points out the move from traditional lab methods to newer diagnostic tools.

Recent Findings

In the past five years, research has focused on creating electrochemical and spectroscopic sensors for real-time monitoring. The review also points out that more nanomaterials are being used to improve sensitivity. It compares contamination levels in farming systems to international standards and finds important gaps in regulations for new types of metalloids.

Summary

The findings show that diagnostic techniques have improved a lot, but they are not widely used in the field yet. The review suggests new directions, like portable sensors and better models for identifying chemical forms. These tools are important for solving global farming challenges and keeping the food supply safe over time.

Graphical Abstract

本文综述了金属和类金属污染物的化学形态、运动和可得性如何影响食品安全和公众健康。它汇集了检测土壤、水和食物中这些污染物的最新进展,并指出了从传统实验室方法到更新诊断工具的转变。最近的发现在过去的五年中,研究的重点是创建用于实时监测的电化学和光谱传感器。这篇综述还指出,更多的纳米材料正在被用于提高灵敏度。它将农业系统中的污染水平与国际标准进行了比较,并发现了对新型金属的监管方面存在的重大差距。研究结果表明,诊断技术已经有了很大的进步,但尚未在该领域得到广泛应用。这篇综述提出了新的方向,比如便携式传感器和更好的识别化学形态的模型。这些工具对于解决全球农业挑战和长期保持食品供应安全至关重要。图形抽象
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引用次数: 0
Mechanism Analysis and Precise Regulation Strategies of Non-Thermal Effects and Synergistic Effects in Microwave Disinfection 微波消毒非热效应与协同效应的机理分析及精准调控策略
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-07-20 DOI: 10.1007/s40726-026-00420-x
Ying-Xiang Fu, Jun-Jie Wang, Hao Wu, Zhi-Cheng Pan, Wei Hu, Ye Du

Purpose of the Review

Microwave disinfection technology is rapidly evolving from traditional thermal treatment to controllable physical field-driven methods. Its disinfection effects in water, solid, and air media can rival or even surpass those of chemical disinfection. By re-examining the long-standing debate around thermal and non-thermal effects, this review systematically summarizes the progress in microwave disinfection research. It aims to provide a theoretical basis and forward-looking directions for the development of precise, efficient, and energy-saving microwave disinfection strategies.

Abstract

This review addresses the ambiguity between thermal and non-thermal effects in microwave disinfection, as well as the lack of quantification regarding their synergistic mechanisms, and proposes a comprehensive conceptual framework. Thermal effects achieve rapid inactivation through volumetric heating of dielectric materials; efficient disinfection can be attained within one minute when temperatures reach or exceed 80°C. When electric field strength exceeds 1.5 kV·m⁻¹ and specific absorption rate (SAR) surpasses 5 kW·kg⁻¹, non-thermal effects can act independently of overall temperature, inducing microbial inactivation via electroporation and intracellular reactive oxygen species generation. Compared to a thermal effect baseline of 0.7-1.4 log reduction, non-thermal effects contribute an additional 1.1-1.8 log inactivation, increasing total inactivation efficiency by 2 to 4 times. Under typical low ionic strength aqueous conditions, the transition between dominant thermal and non-thermal effects is determined by a power density threshold of approximately 60 W·L⁻¹. In microwave-assisted advanced oxidation processes (MW-AOPs), confining radical reactions to the catalyst surface reduces energy consumption to 0.08 kWh·log⁻¹. Furthermore, a classification strategy based on microbial structure has been established: Gram-negative (G⁻) bacteria with high-dielectric-loss outer membranes are best suited for continuous-wave treatment, whereas Gram-positive (G⁺) bacteria require pulsed microwave modulation to penetrate their thick peptidoglycan barrier. This review provides a scientific foundation for the rational design of efficient, low-energy microwave disinfection systems.

Graphical Abstract

微波消毒技术正迅速从传统的热处理技术向可控的物理场驱动技术发展。它在水、固体和空气介质中的消毒效果可以与化学消毒相媲美甚至超过化学消毒。通过重新审视长期以来围绕热效应和非热效应的争论,本文系统地总结了微波消毒的研究进展。旨在为开发精准、高效、节能的微波消毒策略提供理论依据和前瞻性方向。摘要本文针对微波消毒中热效应和非热效应之间的歧义,以及它们的协同机制缺乏量化,提出了一个全面的概念框架。热效应通过介质材料的体积加热实现快速失活;当温度达到或超过80°C时,可在一分钟内实现有效消毒。当电场强度超过1.5 kV·m(毒血症),比吸收率(SAR)超过5 kW·kg(毒血症)时,非热效应可以独立于整体温度发生作用,通过电穿孔和细胞内活性氧的产生导致微生物灭活。与热效应基线减少0.7-1.4对数相比,非热效应可额外减少1.1-1.8对数失活,将总失活效率提高2 - 4倍。在典型的低离子强度水条件下,主要的热效应和非热效应之间的转变是由大约60 W·L⁻¹的功率密度阈值决定的。在微波辅助高级氧化过程(MW-AOPs)中,将自由基反应限制在催化剂表面可将能耗降低到0.08 kWh·log(⁻¹)。此外,一种基于微生物结构的分类策略已经建立起来:具有高介电损耗外膜的革兰氏阴性(G⁺)细菌最适合连续波处理,而革兰氏阳性(G⁺)细菌需要脉冲微波调制才能穿透它们厚厚的肽聚糖屏障。为合理设计高效、低能耗的微波消毒系统提供科学依据。图形抽象
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引用次数: 0
Aerobic Granular Sludge Technology: Challenges and Frontiers in Stability, Scalability, Carbon-Neutral Operation 好氧颗粒污泥技术:稳定性、可扩展性和碳中性操作的挑战和前沿
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-07-09 DOI: 10.1007/s40726-026-00424-7
Tran Thi Thai Hang, Tran Le Luu

Background

Aerobic granular sludge (AGS) is a promising biological wastewater treatment technology owing to its compact footprint, low energy demand, and simultaneous removal of organic matter, nitrogen, and phosphorus. However, despite more than 100 full-scale installations worldwide, major challenges remain in granule stability, large-scale implementation, and carbon-neutral operation.

Methods

This review critically synthesizes evidence from laboratory-, pilot-, and full-scale studies using a Multidimensional Socio-Biological (MSB) framework integrating temporal, spatial, evidence-quality, and governance perspectives. The literature is evaluated across three interconnected themes: granule stability, scalability, and pathways toward carbon-neutral AGS systems.

Results

Three key findings are identified. First, granule disintegration occurs in approximately 42% of full-scale AGS plants annually, highlighting unresolved mechanisms governing long-term stability. Second, the only available full-scale N₂O emission dataset (0.33%) differs by a factor of 5–15 from laboratory estimates (0.54–4.8%), indicating considerable uncertainty in the carbon balance of AGS. Third, no published full-scale AGS studies are available from Southeast Asia, South Asia, or sub-Saharan Africa, despite these regions representing future growth in wastewater treatment infrastructure.

Conclusions

Although AGS has substantial potential for sustainable wastewater treatment, its widespread adoption is constrained by critical evidence gaps. Future research should prioritize long-term full-scale monitoring, greenhouse gas assessment, and demonstration projects in tropical and developing regions to enable reliable and carbon-neutral AGS implementation.

好氧颗粒污泥(AGS)是一种很有前途的生物废水处理技术,因为它占地面积小,能源需求低,同时去除有机物,氮和磷。然而,尽管在全球范围内安装了100多个完整的装置,但在颗粒稳定性、大规模实施和碳中和操作方面仍然存在主要挑战。方法:本综述采用多维社会生物学(MSB)框架,综合时间、空间、证据质量和治理视角,批判性地综合了来自实验室、试点和全面研究的证据。文献通过三个相互关联的主题进行评估:颗粒稳定性,可扩展性和通向碳中性AGS系统的途径。结果确定了三个关键发现。首先,每年约有42%的全规模AGS工厂发生颗粒崩解,这突出了控制长期稳定性的未解决机制。其次,唯一可用的全尺寸N₂O排放数据集(0.33%)与实验室估算值(0.54-4.8%)相差5-15倍,表明AGS的碳平衡存在相当大的不确定性。第三,尽管东南亚、南亚或撒哈拉以南非洲地区代表着未来污水处理基础设施的增长,但没有发表的全面AGS研究。结论尽管AGS具有可持续废水处理的巨大潜力,但其广泛采用受到关键证据空白的限制。未来的研究应优先考虑热带和发展中地区的长期全面监测、温室气体评估和示范项目,以实现可靠和碳中和的AGS实施。
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引用次数: 0
Engineered Biochar for Micro- and Nanoplastic Remediation: Mechanisms, Modifications, and Sustainability 用于微和纳米塑性修复的工程生物炭:机制、修饰和可持续性
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-07-09 DOI: 10.1007/s40726-026-00423-8
Tasmia Falaque, Vivek Kumar Gaur, Yashika Raheja, Chandan Deosthali, Prachi Gaur, Jung-Hwan Kwon, Thanh-Dat Pham, Sunita Varjani

Purpose of Review

Micro- and nanoplastics (MNPs) are an emerging environmental concern, contaminating water, soil, and air and posing risks to ecosystems and human health. Conventional removal techniques, including filtration and coagulation, are often limited by their high costs, energy demands, and secondary pollution. Consequently, Biochar has gained attention as a sustainable alternative due to its high surface area, tuneable properties, and environmental compatibility. Furthermore, existing studies have predominantly focused on laboratory-scale investigations, with limited emphasis on environmental complexity and real-world applicability. This review critically evaluates the potential of engineered biochar for MNPs remediation.

Recent Findings

Recent advances demonstrate that biochar performance can be substantially improved through surface functionalization and pore structure optimization; however, the influence of these modifications on MNPs adsorption mechanisms remains insufficiently understood. This review systematically synthesizes current knowledge on biochar modification strategies, adsorption mechanisms governing MNPs removal, and applications across diverse contaminated environmental matrices. In addition, life cycle assessment (LCA) studies have been critically discussed to evaluate long-term sustainability and environmental implications of biochar-based remediation technologies.

Summary

This review provides a comprehensive perspective on engineered biochar for MNP remediation and identifies current knowledge gaps that limit large-scale implementation. The findings are expected to support the rational design of advanced biochar adsorbents and to facilitate the development of sustainable remediation technologies aligned with circular-economy principles and carbon-neutral objectives.

Graphical Abstract

微塑料和纳米塑料(MNPs)是一种新兴的环境问题,污染水、土壤和空气,并对生态系统和人类健康构成风险。传统的去除技术,包括过滤和混凝,往往受到其高成本,能源需求和二次污染的限制。因此,生物炭作为一种可持续的替代品,由于其高表面积、可调特性和环境相容性而受到关注。此外,现有的研究主要集中在实验室规模的调查,对环境复杂性和现实世界的适用性强调有限。这篇综述批判性地评估了工程生物炭在MNPs修复中的潜力。最近的研究进展表明,生物炭的性能可以通过表面功能化和孔结构优化得到显著改善;然而,这些修饰对MNPs吸附机制的影响仍未得到充分的了解。这篇综述系统地综合了目前关于生物炭改性策略、MNPs去除的吸附机制以及在不同污染环境基质中的应用的知识。此外,生命周期评估(LCA)研究已被批判性地讨论,以评估生物炭基修复技术的长期可持续性和环境影响。本综述提供了工程生物炭用于MNP修复的全面视角,并确定了目前限制大规模实施的知识空白。研究结果有望支持先进生物炭吸附剂的合理设计,并促进符合循环经济原则和碳中和目标的可持续修复技术的发展。图形抽象
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引用次数: 0
Far-UVC (222 nm) in Water Treatment: Disinfection Performance, Micropollutant Degradation, and Implications for Post-Chlorination Disinfection Byproduct Formation 远紫外线(222 nm)在水处理中的消毒性能、微污染物降解以及对氯化后消毒副产物形成的影响
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-07-08 DOI: 10.1007/s40726-026-00425-6
Junlong Peng, Zilong Li, Shuang Wu, Xin Yang, Huang Huang

Purpose of Review

Far-UVC irradiation at 222 nm (UV222), typically emitted by krypton chloride excimer lamps, has emerged as a promising mercury-free platform for water treatment. This review evaluates recent progress in UV222-based water treatment, with conventional 254 nm UV irradiation (UV254) as the primary benchmark, focusing on disinfection, micropollutant degradation, and UV222-induced dissolved organic matter (DOM) transformation in relation to post-chlorination disinfection byproduct (DBP) formation.

Recent Findings

UV222 shows strong disinfection performance against representative bacteria and viruses, although its relative advantage over UV254 is more variable for fungal spores. For micropollutants, compiled paired photolysis data indicate that UV222 generally accelerates direct photolysis relative to UV254, with the enhancement arising from stronger absorptivity, higher quantum yield, or both depending on compound structure. UV222-based advanced processes further broaden the treatment scope beyond direct photolysis through reactive-species-mediated transformation. However, UV222 can also reshape DOM composition and DBP precursor pools. Sole UV222 may reshape DOM molecular composition without large DBP increases, whereas nitrate-containing systems can selectively amplify halonitromethane formation.

Summary

UV222 should not be viewed simply as a more reactive substitute for UV254. Its practical value depends on balancing disinfection and contaminant-removal benefits against matrix-dependent DOM transformation and downstream DBP risks. Future studies should focus on DOM molecular transformation and DBP precursor restructuring, particularly the role of nitrogen incorporation in linking these two processes, as well as realistic treatment-train evaluations.

远紫外线222 nm (UV222)辐射,通常由氯氪准分子灯发出,已成为一种有前途的无汞水处理平台。本文以常规254 nm紫外辐射(UV254)为基准,综述了基于uv222的水处理的最新进展,重点介绍了uv222的消毒、微污染物降解以及与氯化后消毒副产物(DBP)形成有关的uv222诱导溶解有机物(DOM)转化。最近的发现suv222对代表性细菌和病毒表现出较强的消毒性能,尽管其相对于UV254的优势在真菌孢子方面变化较大。对于微污染物,编译的成对光解数据表明,相对于UV254, UV222通常加速直接光解,其增强取决于化合物结构,吸收率更强,量子产率更高,或两者兼而有之。基于uv222的先进工艺进一步拓宽了通过反应-物种介导转化直接光解以外的处理范围。然而,UV222也可以重塑DOM组成和DBP前体池。鞋底UV222可以重塑DOM分子组成,而不需要增加DBP,而含硝酸盐的体系可以选择性地放大卤硝基甲烷的形成。yuv222不应被简单地视为UV254的反应性更强的替代品。它的实用价值取决于在消毒和去除污染物的好处与依赖于基质的DOM转换和下游DBP风险之间取得平衡。未来的研究应侧重于DOM分子转化和DBP前体重组,特别是氮掺入在连接这两个过程中的作用,以及现实的治疗训练评价。
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引用次数: 0
Correction: Bioelectrochemical Enhancement of Antibiotics Removal from Mariculture Wastewater: A Critical Review 修正:生物电化学强化去除海水养殖废水中的抗生素:综述
IF 9.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2026-07-04 DOI: 10.1007/s40726-026-00422-9
Haoran Xin, Jieling Li, Qingjuan Fan, Wenchao Xue, Allan Sriratana Tabucanon, Haiping Luo, Guangli Liu
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引用次数: 0
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Current Pollution Reports
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