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Sustainable Ca-TiO₂ Paper Platforms: Exploiting Eggshell Biowaste for Environmental Remediation 可持续的Ca-TiO 2纸平台:利用蛋壳生物废弃物进行环境修复
IF 8.131 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-01-05 DOI: 10.1039/d5en00864f
Beatrice Canova, Maria Leonor Leonor Matias, Maria Magalhães, Ana Pimentel, Andreia Matzinhe, Catarina Pinto Reis, Jonas Deuermeier, Rodrigo Matins, Elvira Fortunato, Chiara Bisio, Daniela Nunes
Sustainable photocatalysis has emerged as a promising approach for environmental remediation by combining efficiency with green chemistry principles. In this study, Ca-TiO₂ photocatalytic platforms were developed using cellulose paper as a substrate, calcium sourced directly from eggshell biowaste, and a sustainable microwave-assisted synthesis approach. A novel functionalization of the Whatman paper preserved its structural integrity at temperatures above 200 °C, enabling the direct growth of TiO₂ nanomaterials on paper substrate without any post-synthesis treatment. Incorporation of bio-derived Ca²⁺ modified the TiO₂ structure, inducing structural defects that included lattice distortions, voids, and surface step sites, modifying optical absorption, and enhancing surface hydroxylation. The resulting Ca-TiO₂ paper-based platforms efficiently degraded tetracycline, achieving over 80 % removal under solar irradiation in 150 minutes, corresponding to a photodegradation rate 1.3 times higher than that of pure TiO₂. Reusability and ecotoxicity tests confirmed their stability and safety for long-term environmental applications. By integrating waste valorization, green synthesis, and defect engineering, this work demonstrates a sustainable and scalable strategy for producing high-performance photocatalytic platforms, aligning with circular economy principles and offering potential solutions for global water pollution challenges.
可持续光催化已成为一种很有前途的环境修复方法,它将效率与绿色化学原理相结合。在本研究中,以纤维素纸为底物,直接从蛋壳生物废物中获取钙,并采用可持续的微波辅助合成方法,开发了Ca-TiO 2光催化平台。一种新的功能化的Whatman纸在200 °C以上的温度下保持其结构完整性,使二氧化钛纳米材料无需任何合成后处理即可直接在纸基上生长。生物来源的Ca 2⁺修饰了TiO 2结构,诱发了结构缺陷,包括晶格畸变、空隙和表面台阶位点,修饰了光学吸收,增强了表面羟基化。所得到的Ca-TiO 2纸基平台有效地降解了四环素,在150分钟的太阳照射下,脱除率超过80% %,和光降解率比纯TiO 2高1.3倍。可重复使用性和生态毒性测试证实了它们在长期环境应用中的稳定性和安全性。通过整合废物增值、绿色合成和缺陷工程,这项工作展示了一种可持续和可扩展的战略,用于生产高性能光催化平台,符合循环经济原则,并为全球水污染挑战提供潜在的解决方案。
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引用次数: 0
Synergistic adsorption and oxidation of Sb(III) from mining wastewater using hybrid ZIF-8-Fe nanoparticles: Performance and mechanisms ZIF-8-Fe复合纳米颗粒协同吸附氧化矿山废水中Sb(III)的性能与机理
IF 8.131 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-01-05 DOI: 10.1039/d5en01008j
Shiyi Tu, Wenpeng Li, Yangyang Xu, Li Gan, Xiulan Weng, Zuliang Chen
The increasing release of antimony (Sb) into water environments due to anthropogenic activities poses significant ecological risks. This study developed a novel hybrid material, zeolitic imidazolate framework-8-iron nanoparticles (ZIF-8-Fe NPs), which demonstrates a synergistic adsorption-oxidation mechanism for efficient removal of Sb(III) from aqueous solutions. Major findings reveal that at an initial Sb(III) concentration of 1 mg L-1, ZIF-8-Fe NPs achieved a 73.3% removal efficiency within three hours through the dual processes of direct adsorption and oxidation of Sb(III) to Sb(V). Scanning electron microscopy-energy dispersive spectrometry (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS) revealed that the removal mechanism involved both direct adsorption of Sb(III) by ZIF-8-Fe NPs and oxidation of Sb(III) to Sb(V), with two distinct morphologies of Sb adsorbed on the surface. The formation of covalent bonds (Zn-OH-Sb and Fe-O-Sb) was identified as the key factor in removing both Sb(III) and Sb(V) from aqueous solutions. The adsorption process conformed to the Langmuir adsorption isotherm and pseudo-second-order kinetics, with correlation coefficients (R²) of 0.959 and 0.999, respectively. The proposed mechanism suggests that the formation of Zn-OH-Sb and Fe-O-Sb covalent bonds plays a crucial role in Sb(III) removal. Significantly, ZIF-8-Fe NPs achieved removal efficiencies of 91.5% and 94.8% for Sb(III) at environmentally relevant concentrations of 100 µg L-1 and 20 µg L-1, in actual mining wastewater, demonstrating its practical applicability. This study establishes that ZIF-8-Fe NPs constitute an effective nanomaterial with significant potential for Sb(III) remediation in wastewater.
由于人类活动,锑(Sb)向水环境释放的增加构成了重大的生态风险。本研究开发了一种新型的杂化材料,沸石咪唑酸框架-8-铁纳米颗粒(ZIF-8-Fe NPs),该材料展示了一种协同吸附-氧化机制,可有效去除水溶液中的Sb(III)。结果表明,在初始Sb(III)浓度为1 mg L-1时,ZIF-8-Fe NPs通过直接吸附和氧化Sb(III)生成Sb(V)的双重过程,在3小时内达到73.3%的去除率。扫描电镜-能谱分析(SEM-EDS)、傅里叶变换红外光谱(FTIR)和x射线光电子能谱分析(XPS)表明,ZIF-8-Fe纳米粒子对Sb(III)的直接吸附和Sb(III)的氧化生成Sb(V)的去除机制均参与其中,表面吸附了两种不同形态的Sb。共价键的形成(Zn-OH-Sb和Fe-O-Sb)被确定为从水溶液中去除Sb(III)和Sb(V)的关键因素。吸附过程符合Langmuir等温线和拟二级吸附动力学,相关系数(R²)分别为0.959和0.999。该机制表明,Zn-OH-Sb和Fe-O-Sb共价键的形成对Sb(III)的去除起着至关重要的作用。值得注意的是,ZIF-8-Fe NPs在环境相关浓度为100 μ g L-1和20 μ g L-1时,对实际采矿废水中Sb(III)的去除率分别为91.5%和94.8%,显示了其实用性。本研究表明,ZIF-8-Fe纳米粒子是一种有效的纳米材料,具有修复废水中Sb(III)的巨大潜力。
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引用次数: 0
Tritopic Linker-Integrated Fluorescent Bismuth Nanosheets for Sensitive Pesticide Detection in Agricultural Samples 用于农业样品中农药敏感检测的三配位连接物集成荧光铋纳米片
IF 8.131 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-01-03 DOI: 10.1039/d5en00467e
Deepak Dabur, Ya-Ching Chang Chien, Priyanka Rana, Hui-Fen Wu
A highly stable luminescent sensor based on bismuth-based organic nanosheets, Bi(TMA), has been developed for the rapid visual detection of the toxic pesticide dichloran (DCN) in real food matrices. Bi(TMA) is constructed from Bi(III) ions and the tridentate linker trimesic acid (TMA), yielding a two‑dimensional interpenetrated architecture stabilized by extensive O‑bridging coordination bonds. The framework's structural stability is attributed to carboxylic coordination and its interpenetrated architecture, which endows the nanosheets with high fluorescence stability in dimethyl sulfoxide (DMSO) across a wide pH range for up to 30 days. Under excitation at 370 nm, Bi(TMA) displays a sharp emission maximum at 452 nm, which is selectively quenched by DCN in DMSO at pH=6.5, while remaining unchanged in the presence of a broad panel of competing pesticides. Selectivity originates from the formation of a highly stable Bi(TMA)-DCN complex mediated by imine bond formation and subsequent charge‑transfer interactions, as confirmed by different types of data collecting from different instruments including TRPL and (Zeta)ζ‑potential measurements. The sensor exhibits a detection limit of 0.03 nM, surpassing the performance of recently reported metal-organic framework (MOF)-based sensors. In spiked environmental and food samples, recoveries range from 88 % to 115 % with relative standard deviations ≤ 4 %, demonstrating the practicality of Bi(TMA) for on‑site pesticide monitoring. This work provides a straightforward design strategy for bismuth‑based luminescent nanosheets with tunable photophysical properties and high analytical performance.
基于铋基有机纳米片Bi(TMA)研制了一种高稳定性的发光传感器,用于快速视觉检测实际食品基质中的有毒农药二氯胺(DCN)。Bi(TMA)是由Bi(III)离子和三羧酸(TMA)构成的,形成了由广泛的O桥接配位键稳定的二维互穿结构。该框架的结构稳定性归因于羧基配位及其互穿结构,这使得纳米片在二甲基亚砜(DMSO)中具有高荧光稳定性,可在宽pH范围内长达30天。在370 nm的激发下,Bi(TMA)在452 nm处显示出最大的发射峰,在pH=6.5的DMSO中被DCN选择性猝灭,而在广泛的竞争农药存在下保持不变。选择性源于由亚胺键形成和随后的电荷转移相互作用介导的高度稳定的Bi(TMA)-DCN复合物的形成,正如来自不同仪器(包括TRPL和(Zeta)ζ电位测量)的不同类型的数据收集所证实的那样。该传感器的检测限为0.03 nM,超过了最近报道的基于金属有机框架(MOF)的传感器的性能。在加标环境和食品样品中,回收率为88 % ~ 115 %,相对标准偏差≤ 4 %,证明了Bi(TMA)用于现场农药监测的实用性。这项工作为具有可调光物理性质和高分析性能的铋基发光纳米片提供了一种简单的设计策略。
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引用次数: 0
Co-assembly of Structurally Different Biomacromolecules-modified Maghemite Nanoparticles with Nitrate Sequestration Potential 结构不同的生物大分子修饰磁赤铁矿纳米颗粒与硝酸盐固存电位的共组装
IF 8.131 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-01-02 DOI: 10.1039/d5en01037c
Hui Dong, Bo Su, YanXi Cheng, Saikat Ghosh, Nihar Ranjan Pradhan, Bo Pan, Baoshan Xing
The co-assembly of humic acid (HA)-coated maghemite nanoparticles (H-GFeNPs) and bovine serum albumin (BSA)-modified maghemite nanoparticles (B-GFeNPs) and sequestration of NO₃⁻ within the colloidal crystals were investigated. The π-π interaction between aromatic moieties of the adsorbed BSA and HA controlled the co-assembly process. The 1:1 binary mixture of H-GFeNPs and B-GFeNPs at pH 4 showed screw dislocation-driven growth of colloidal crystals, especially at higher concentrations of NO₃⁻. But, at pH 7, the binary mixture in the presence of NO₃⁻ produced spherical dendritic nanostructures and hierarchical growth of dendrites. However, at higher levels of NO3-, the binary mixture produced 2D cubic lattice and rocksalt-like 3D colloidal crystals. In addition, we also detected the growth of dendrites, ubiquitous in rocksalt-type crystal growth, specifically in an unsaturated environment. The binding of NO₃⁻ to the hydrophobic and positively charged residues of the protein, supplemented by the loss of α-helix and reduced radius of gyration (Rg), possibly favored crystal growth. Signatures of the NO3- specific Raman bands within the colloidal crystals discerned the sequestration of the highly mobile contaminant ion within the crystalline domain. Therefore, potentially diminishes the atmospheric emission of high global warming potential (GWP) oxides of N produced via denitrification.
研究了腐殖酸(HA)包覆的磁赤铁矿纳米粒子(H-GFeNPs)和牛血清白蛋白(BSA)修饰的磁赤铁矿纳米粒子(B-GFeNPs)的共组装和NO₃⁻在胶体晶体内的吸附。吸附的BSA和HA的芳香基团之间的π-π相互作用控制了共组装过程。H-GFeNPs和B-GFeNPs的1:1混合物在pH为4时显示出螺旋位错驱动的胶体晶体生长,特别是在更高浓度的NO₃⁻下。但是,在pH为7时,在NO₃⁻的存在下,这种二元混合物产生了球形的枝晶纳米结构和枝晶的分层生长。然而,在较高的NO3-水平下,二元混合物产生二维立方晶格和岩盐状三维胶体晶体。此外,我们还检测到树突的生长,在岩盐型晶体生长中普遍存在,特别是在不饱和环境中。NO₃与蛋白质的疏水和带正电的残基的结合,加上α-螺旋的损失和旋转半径(Rg)的减小,可能有利于晶体的生长。胶体晶体内NO3-特异性拉曼谱带的特征识别了晶体区域内高流动性污染离子的隔离。因此,潜在地减少了通过反硝化产生的高全球变暖潜能值(GWP)氮氧化物的大气排放。
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引用次数: 0
Innovative green nanotechnology for sustainable water purification under climate change: tackling antibiotic contaminants 气候变化下可持续水净化的创新绿色纳米技术:处理抗生素污染物
IF 5.1 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-01-02 DOI: 10.1039/D5EN00956A
Nawagamuwage Harshani Madushika, Imalka Munaweera, Gayani Yasodara Liyanage, Pradeepa Jayawardane and Pathmalal Marakkale Manage

Antibiotic contamination represents a pressing environmental crisis affecting aquatic ecosystems globally, a challenge that climate change only intensifies. Key culprits of this pollution include pharmaceutical discharges, agricultural runoff, and improper waste disposal. These antibiotics persist in our water systems due to their stable chemical structures, while climate-related factors like rising temperatures and extreme weather can exacerbate their impact. The accumulation of these substances poses significant threats to aquatic life, human health, and the broader environment, as they facilitate the alarming spread of antimicrobial resistance among microorganisms. Unfortunately, traditional water treatment methods remain largely ineffective against these stubborn pollutants. In response to this growing issue, green nanotechnology emerges as a promising and sustainable solution. By harnessing plant extracts, microbes, and agricultural waste for the synthesis of nanoparticles, this approach minimizes environmental harm while effectively addressing contamination. Metal oxide nanoparticles, carbon-based materials, and biopolymeric nanomaterials have proven to be highly efficient in eliminating antibiotics through processes such as adsorption, photodegradation, and redox reactions. However, the effectiveness and applicability of these nanoparticles under varying climate conditions warrant further exploration. This review highlights the transformative potential of green nanotechnology for safe and sustainable water remediation. It underscores recent advancements in eco-friendly nanomaterials, elucidating their removal mechanisms, environmental behavior, and the critical need for climate-resilient, safe-by-design strategies. To combat antibiotic pollution effectively amid shifting climatic conditions, we must investigate green nanotechnology for future water treatment practices. This proactive approach not only safeguards our water systems but also ensures a healthier future for both aquatic ecosystems and human communities.

抗生素污染是影响全球水生生态系统的紧迫环境危机,气候变化只会加剧这一挑战。造成这种污染的罪魁祸首包括药品排放、农业径流和不当的废物处理。这些抗生素由于其稳定的化学结构而持续存在于我们的水系统中,而与气候有关的因素,如气温上升和极端天气,会加剧它们的影响。这些物质的积累对水生生物、人类健康和更广泛的环境构成重大威胁,因为它们促进了微生物中抗菌素耐药性的惊人传播。不幸的是,传统的水处理方法对这些顽固的污染物仍然基本上无效。为了应对这一日益严重的问题,绿色纳米技术作为一种有前途的可持续解决方案出现了。通过利用植物提取物、微生物和农业废弃物合成纳米颗粒,这种方法在有效解决污染问题的同时,最大限度地减少了对环境的危害。金属氧化物纳米颗粒、碳基材料和生物聚合物纳米材料已被证明通过吸附、光降解和氧化还原反应等过程在消除抗生素方面非常有效。然而,这些纳米颗粒在不同气候条件下的有效性和适用性值得进一步探索。这篇综述强调了绿色纳米技术在安全和可持续的水修复方面的变革潜力。它强调了生态友好型纳米材料的最新进展,阐明了它们的去除机制、环境行为以及对气候适应性强、设计安全策略的迫切需求。为了在不断变化的气候条件下有效地对抗抗生素污染,我们必须为未来的水处理实践研究绿色纳米技术。这种积极主动的方法不仅保护了我们的水系统,而且确保了水生生态系统和人类社区更健康的未来。
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引用次数: 0
Electroanalytical Overview: Recent Advances in the Sensing of Arsenic Using Screen-Printed Electrochemical Platforms 电分析综述:利用丝网印刷电化学平台检测砷的最新进展
IF 8.131 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-01-02 DOI: 10.1039/d5en00708a
Jessica L Pimlott, Dale Brownson, Edward Peter Randviir, Eric Brack, Craig E. Banks, Samuel James Rowley-Neale
Access to clean drinking water remains a critical global health issue, with over 2 billion people lacking access to safely managed water. Among the contaminants of concern, heavy metals-particularly arsenic-pose significant risks due to their persistence and toxicity. Long-term exposure to arsenic (As 3+ ), especially at concentrations exceeding the World Health Organisation's (WHO) guideline of 10 µg/L, has been linked to severe health conditions, including cancer, dermatological issues, and cognitive impairments. Traditional laboratory-based approaches offer high sensitivity and selectivity but are expensive, time-consuming, and require skilled personnel, making them impractical for in-the-field use.In recent years, electrochemical methods, particularly using screen-printed electrodes (SPEs), have emerged as a promising alternative for As 3+ detection, the most toxic form. SPEs offer a compact, costeffective, and portable solution, enabling real-time, on-site monitoring of arsenic levels in water. This review systematically explores recent advancements in SPEs for the detection of As³⁺, with a focus on electrode modifications aimed at enhancing sensitivity and selectivity. We highlight techniques involving the integration of precious metals, biosensors, and carbon-based materials, all of which contribute to improved (lower) detection limits and wide sensing ranges. Practical applications in environmental monitoring-particularly in remote or resource-limited settings-are also discussed, offering a scalable and efficient solution for arsenic detection; SPEs have the potential to revolutionise water quality assessment and supporting global public health initiatives.
获得清洁饮用水仍然是一个关键的全球健康问题,有20多亿人无法获得安全管理的水。在令人担忧的污染物中,重金属——尤其是砷——由于其持久性和毒性而构成重大风险。长期接触砷(As 3+),特别是浓度超过世界卫生组织(世卫组织)10微克/升的指导标准时,与严重的健康状况有关,包括癌症、皮肤病和认知障碍。传统的基于实验室的方法具有高灵敏度和选择性,但成本高,耗时长,并且需要熟练的人员,因此不适合现场使用。近年来,电化学方法,特别是使用丝网印刷电极(spe),已经成为一种有希望的替代砷3+检测的方法,砷3+是毒性最大的形式。spe提供了一种紧凑、经济、便携的解决方案,能够实时、现场监测水中的砷含量。这篇综述系统地探讨了用于检测As³⁺的spe的最新进展,重点是电极修饰,旨在提高灵敏度和选择性。我们强调涉及贵金属,生物传感器和碳基材料集成的技术,所有这些都有助于提高(更低)检测限和更宽的传感范围。还讨论了环境监测的实际应用,特别是在偏远或资源有限的环境中,为砷检测提供了可扩展和有效的解决方案;spe具有彻底改变水质评估和支持全球公共卫生倡议的潜力。
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引用次数: 0
Portable gold nanoparticle-based colorimetric sensor for rapid on-site detection of glyphosate herbicide in plants and soil 基于金纳米粒子的便携式草甘膦除草剂快速现场检测比色传感器
IF 5.1 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-01-02 DOI: 10.1039/D5EN00748H
Fabian Mares-Briones, Dulce Correa-González, Edson Jiménez-Ameneyro, J. Luis López-Miranda, Alberto Elizalde-Mata, Miriam Estévez and Rodrigo Esparza

Detecting glyphosate (Gly), a widely used herbicide in agricultural practice worldwide, is crucial due to its environmental impact and potential health risks. This study presents a colorimetric sensor based on gold nanoparticles (AuNPs) functionalized with cysteamine (AuNPs + Cys) for Gly-sensitive and selective detection. The AuNPs were synthesized using the Turkevich method and characterized using ultraviolet-visible spectroscopy (UV-vis), dynamic light scattering, X-ray diffraction spectroscopy, and scanning electron microscopy. The AuNPs display a localized surface plasmon resonance peak at a 520 nm wavelength and have an average size distribution of 23 nm with good dispersion. The AuNPs + Cys exhibit unique optical properties, allowing for visible color changes in response to varying concentrations of Gly. The detection mechanism relies on the interaction between Gly and the Cys on the nanoparticle surface, which induces changes in the aggregation state of the AuNPs, leading to a shift in the UV-vis absorption spectrum. The sensor was tested at a maximum concentration of 100 ppm Gly, with a detection limit of 1.42 ppm and a distinct color change easily visible to the naked eye. To evaluate the sensor's selectivity, assays were conducted in a soil matrix. Glufosinate was employed as a complementary analyte, and the sensor exhibited a clear differentiation, thus achieving selective detection between the herbicides. The developed AuNPs + Cys sensor offers a simple, cost-effective, and efficient method for Gly detection, with potential applications in environmental monitoring and agricultural practices.

草甘膦是一种在世界范围内广泛使用的除草剂,由于其对环境的影响和潜在的健康风险,检测草甘膦至关重要。本研究提出了一种基于半胱胺功能化金纳米颗粒(AuNPs+Cys)的比色传感器,用于甘氨酸敏感和选择性检测。采用Turkevich法合成了AuNPs,并利用紫外可见光谱(UV-Vis)、动态光散射、x射线衍射光谱和扫描电镜对其进行了表征。AuNPs在520 nm波长处显示出局域表面等离子体共振峰,平均尺寸分布为23 nm,色散良好。AuNPs+Cys表现出独特的光学特性,允许可见光颜色随不同浓度的Gly而变化。检测机制依赖于纳米颗粒表面的Gly和Cys之间的相互作用,这种相互作用会引起AuNPs聚集状态的变化,从而导致紫外-可见吸收光谱的偏移。该传感器在最大浓度为100 ppm Gly的条件下进行了测试,检测限为1.42 ppm,肉眼很容易看到明显的颜色变化。为了评估传感器的选择性,在土壤基质中进行了测定。草甘膦作为补充分析物,传感器表现出明显的分化,从而实现了除草剂之间的选择性检测。开发的AuNPs+Cys传感器提供了一种简单、经济、高效的Gly检测方法,在环境监测和农业实践中具有潜在的应用前景。
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引用次数: 0
Sustainable Mitigation of Chromium Bioavailability in Soil and Rice Grain Using nZVI-Biochar: An Integrated Approach for Remediation and Enhanced Nutrition 利用nzvi -生物炭可持续降低土壤和稻米中铬的生物有效性:一种综合修复和增强营养的方法
IF 8.131 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-26 DOI: 10.1039/d5en00790a
Gourav Mondal, Sonali Banerjee, Shreya Chakraborty, KASTURI CHARAN, Pradip Bhattacharyya
Chromium (Cr) contamination in soils of rice-growing regions poses a significant risk to both human health and the environment. Elevated Cr level in soil reduces photosynthetic activity, induces oxidative stress, and limits rice plant growth. This work investigated the remediation of Cr-contaminated soil using bare nZVI (NC), biochar (BC), and biochar-supported nZVI (ZB) and examined their impacts on plant development, Cr uptake, and micronutrient (Zn and Fe) accumulation in rice grains. The result indicates nZVI-biochar significantly reduced bioavailable Cr in soil [water-soluble (F1) = 71%, exchangeable (F2) = 73%, and oxide-bound (F4) = 64%)], which is primarily transformed into unavailable forms. Therefore, the application of nZVI-biochar composites effectively inhibits Cr mobility in the soil. Also, Cr accumulation in rice grain was considerably reduced in the ZB additions (79%), as compared to the untreated soil. Although BC and NC alone improved plant performance in contaminated soil, their combination was more effective. The use of ZB, NC, and BC at 5000 mg kg-1 increased grain Fe content by 91%, 81%, and 51% respectively. Additionally, biochar in ZB increased grain Zn by 34%, likely due to its low Zn sorption affinity, facilitating Zn transportation and accumulation. Overall, application of ZB at 5000 mg kg-1 enhanced rice growth, biomass, photosynthetic pigments, and improved antioxidant enzyme activity while Cr in the soil, and thereby lowering its absorption and translocation to grains. Hence, amending soil with a ZB composite may offer a promising approach for the safe utilization of Cr-contaminated sites in the future.
水稻种植区土壤中的铬污染对人类健康和环境都构成重大风险。土壤中铬含量升高会降低水稻的光合活性,诱发氧化应激,限制水稻的生长。研究了裸氮化锌(NC)、生物炭(BC)和生物炭负载氮化锌(ZB)对Cr污染土壤的修复效果,并研究了它们对植物发育、Cr吸收和水稻籽粒微量元素(Zn和Fe)积累的影响。结果表明,nzvi -生物炭显著降低了土壤中生物可利用Cr[水溶性(F1) = 71%,可交换性(F2) = 73%,氧化结合(F4) = 64%],主要转化为不可用形式。因此,施用nzvi -生物炭复合材料可以有效抑制土壤中Cr的流动性。此外,与未处理的土壤相比,添加ZB显著降低了水稻籽粒中Cr的积累(79%)。虽然单独施用BC和NC能提高污染土壤中植物的生长性能,但两者联合施用效果更好。5000mg kg-1添加ZB、NC和BC,籽粒铁含量分别提高91%、81%和51%。此外,生物炭对锌的吸附亲和力较低,有利于锌的运输和积累,可使籽粒锌增加34%。总体而言,施用5000 mg kg-1 ZB可促进水稻生长、生物量、光合色素,提高土壤中Cr的抗氧化酶活性,从而降低其对籽粒的吸收和转运。因此,用ZB复合材料修复土壤可能是未来安全利用铬污染场地的一种有前途的方法。
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引用次数: 0
Copper oxide nanoparticles mitigate cadmium-arsenic phytotoxicity to rice plants (O.sativa) and protect Daphnia magna via soil-water partitioning 氧化铜纳米颗粒减轻镉砷对水稻的植物毒性,并通过土壤-水分配保护大水蚤
IF 8.131 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-23 DOI: 10.1039/d5en01106j
Xingyu Yan, Jing Liu, Wenhui Li, Jiayi Su, Jiawei Wang, Zhongxiang Cao
Serving as a staple food for over half of the world population, rice plants tend to accumulate higher levels of cadmium (Cd) and arsenic (As) than other cereal crops. Copper oxide nanoparticles (nCuO), known for their stability and adsorption capacity, show potential for remediating soils contaminated with Cd and As. This study investigated the regulatory effects of nCuO on rice (O.sativa) seedling growth under combined Cd-As stress and the potential detoxification efficacy of nCuO for Cd and As via soil-water partitioning in two distinct soil environments, i.e., acidic organic-rich red soils and neutral high cation-exchange-capacity (CEC) brown soils. Results demonstrated that nCuO at 10–100 mg L-1 alleviated oxidative stress caused by Cd-As and promoted seedling growth. In particular, nCuO reduced Cd-As accumulation in rice seedlings grown in the brown soils by inhibiting the expression of related genes OsNRAMP5 and OsLsi1. However, in the red soil, greater mobility of Cd-As resulted in their higher root accumulation and stronger antioxidant responses in rice seedlings, requiring higher doses of nCuO to achieve effective remediation. Furthermore, nCuO reduced the toxicity of simulated drainage water to Daphnia magna, showing its efficacy in mitigating ecological risks associated with Cd-As partitioning from contaminated soils to aquatic ecosystems. This alleviation was more effective in the brown soils. These findings provide insights into the mechanisms by which nCuO mitigates Cd-As co-stress in rice, and nCuO behaviors in contrasting soil environments for remediating contaminated paddy fields and the adjacent water environments.
作为世界上一半以上人口的主食,水稻往往比其他谷类作物积累更高水平的镉(Cd)和砷(as)。氧化铜纳米粒子(nCuO)以其稳定性和吸附能力而闻名,显示出修复镉和砷污染土壤的潜力。本研究在酸性富有机红壤和中性高阳离子交换容量(CEC)棕壤两种不同土壤环境下,研究了nCuO对Cd-As复合胁迫下水稻幼苗生长的调控作用,以及nCuO通过土壤-水分配对Cd和As的潜在解毒效果。结果表明,10 ~ 100 mg L-1的nCuO可减轻Cd-As引起的氧化应激,促进幼苗生长。特别是,nCuO通过抑制相关基因OsNRAMP5和OsLsi1的表达,减少了棕色土壤中水稻幼苗Cd-As的积累。然而,在红壤中,Cd-As的流动性越大,导致其在水稻幼苗中的根积累量越大,抗氧化反应也越强,因此需要更高剂量的nCuO才能实现有效的修复。此外,nCuO降低了模拟排水对大水蚤的毒性,显示了其在减轻Cd-As从污染土壤向水生生态系统分配相关的生态风险方面的有效性。这种缓解在棕色土壤中更为有效。这些发现揭示了nCuO缓解水稻Cd-As共胁迫的机制,以及nCuO在不同土壤环境下修复受污染稻田和邻近水环境的行为。
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引用次数: 0
When does the aggregation matter? The CLUMP scheme for classifying nanoparticles based on the influence of aggregation on environmental fate 聚合什么时候起作用?基于聚集对环境命运影响的聚类方案对纳米颗粒进行分类
IF 8.131 2区 环境科学与生态学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-12-23 DOI: 10.1039/d5en00950b
Szymon Swiatek Brzezinski, Michal Kalapus, Tomasz Puzyn
Engineered nanoparticles (ENPs) released into aquatic environments can undergo multiple removal processes, including dissolution, sedimentation, advection, and aggregation with natural particles. This study quantitatively assesses the probability that heteroaggregation is the dominant removal pathway among these mechanisms. The aggregation propensity of 36 ENP types was evaluated by estimating attachment efficiencies (α) derived from DLVO theory across a wide range of environmental conditions. Results show that α decreases with particle size at low Hamaker constants but increases with size at higher values. The calculated α values were incorporated into an environmental fate model to quantify the relative importance of aggregation versus other removal processes. Aggregation dominance probabilities varied widely among ENPs - from a few percent to 100% - depending on material composition, particle size, and zeta potential. Based on these outcomes, a five-tier CLUMP classification was developed to categorize ENPs according to the frequency of heteroaggregation dominance. This classification framework provides a comparative measure of nanomaterial mobility and environmental stability, offering a practical tool to support environmental fate modeling and risk assessment.
工程纳米颗粒(ENPs)释放到水生环境中可以经历多种去除过程,包括溶解、沉淀、平流和与天然颗粒聚集。本研究定量评估了异聚集是这些机制中主要的去除途径的可能性。根据DLVO理论估算了36种ENP类型在不同环境条件下的附着效率(α),从而评估了它们的聚集倾向。结果表明,当Hamaker常数较低时,α随粒径的增大而减小,当Hamaker常数较高时,α随粒径的增大而增大。计算出的α值被纳入环境命运模型,以量化聚集与其他去除过程的相对重要性。聚合优势概率在ENPs之间变化很大——从百分之几到百分之百——取决于材料组成、颗粒大小和zeta势。基于这些结果,建立了一个五层的聚类分类,根据异聚集优势的频率对enp进行分类。该分类框架提供了纳米材料流动性和环境稳定性的比较措施,为支持环境命运建模和风险评估提供了实用工具。
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引用次数: 0
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Environmental Science: Nano
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