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Environmentally-friendly activated carbon for the removal of antibiotic-resistant bacteria removal from hospital wastewater 环保型活性炭去除医院废水中的耐药菌
Q1 Environmental Science Pub Date : 2025-07-16 DOI: 10.1016/j.enmm.2025.101088
Ederaldo Luiz Beline , Alexandre Amado de Moura , Alexandre Diório , Anna Carla Ribeiro , Benício Alves de Abreu Filho , Daniel Tait Vareschini , Débora Federici dos Santos , Leidiane Silva Vasconcelos , Rosângela Bergamasco , Maria Angélica Simões Dornellas de Barros
The rise of antibiotic-resistant bacteria has driven research into natural antimicrobial alternatives. Allicin, a compound formed in freshly crushed garlic cloves, exhibits antibacterial properties but suffers from poor stability in aqueous environments. That is why this study aimed to explore the synthesis and characterization of allicin-modified activated carbon (AMAC) and evaluate its potential application removing Escherichia coli from synthetic hospital wastewater (HWW). Sugarcane bagasse (SB) provided by a local Brazilian alcohol mill was transformed into activated carbon (SBAC) through a hydrothermal process (heating at 200 °C for 24 h followed by activation at 450 °C for 10 min). Allicin extract was obtained from fresh garlic and impregnated onto the SBAC surface, resulting in AMAC with 105 µm mean diameter. The materials were characterized (FT-IR, Raman and N2-physisorption), revealing significant structural and surface modifications. The antibacterial activity of allicin against E. coli was assessed through minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) trials and disk diffusion, demonstrating effective bacterial growth inhibition, as expected. Adsorption assays showed that AMAC enhanced E. coli removal efficiency in synthetic HWW by 3 %, compared to the AMAC in deionized and sterile water. This improvement was attributed to the positive interactions and synergistic effects between AMAC and the wastewater constituents. In other words, it means that AMAC can be used in the E. coli removal even in presence of organic and inorganic molecules without any loss of efficiency. The study also highlights the environmentally friendly synthesis process of AMAC and its potential as a sustainable solution for treating HWWs without the use of antibiotics, thus avoiding the potential release of pharmaceutical compounds into the environment. The results suggest that AMAC could be a viable alternative for enhancing the removal of antibiotic-resistant bacteria from contaminated water sources, contributing to public health and environmental protection.
耐抗生素细菌的增加推动了对天然抗菌替代品的研究。大蒜素是一种在新鲜碾碎的蒜瓣中形成的化合物,具有抗菌性能,但在水环境中稳定性差。因此,本研究旨在探索大蒜素修饰活性炭(AMAC)的合成和表征,并评估其在去除医院合成废水(HWW)中大肠杆菌的潜在应用。通过水热法(在200℃下加热24 h,然后在450℃下活化10 min)将巴西当地一家酒精厂提供的甘蔗渣(SB)转化为活性炭(SBAC)。从新鲜大蒜中提取大蒜素,并将其浸渍在SBAC表面,得到平均直径为105µm的AMAC。对材料进行了表征(FT-IR, Raman和n2 -物理吸附),揭示了明显的结构和表面修饰。通过最小抑菌浓度(MIC)试验、最小杀菌浓度(MBC)试验和圆盘扩散试验,对大蒜素对大肠杆菌的抑菌活性进行了评价,结果表明,大蒜素对大肠杆菌的生长具有抑制作用。吸附实验表明,与AMAC在去离子水和无菌水中相比,AMAC在合成水中对大肠杆菌的去除效率提高了3%。这种改善归因于AMAC与废水成分之间的积极相互作用和协同效应。换句话说,这意味着即使存在有机和无机分子,AMAC也可以用于去除大肠杆菌,而不会损失任何效率。该研究还强调了AMAC的环境友好型合成工艺及其作为不使用抗生素治疗hww的可持续解决方案的潜力,从而避免了药物化合物可能释放到环境中。结果表明,AMAC可能是一种可行的替代方法,可以加强对受污染水源中抗生素耐药细菌的去除,有助于公共卫生和环境保护。
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引用次数: 0
Detoxification of wastewater with toxic cyanide substance using TiO2-based photocatalysts 二氧化钛基光催化剂对含有毒氰化物废水的解毒研究
Q1 Environmental Science Pub Date : 2025-07-11 DOI: 10.1016/j.enmm.2025.101087
Erkan Cakiroglu , Suleyman Demir , Erdal Celik
Industrial, agricultural, and domestic chemicals increasingly pollute the environment, affecting water, air, and soil even at low concentrations. This pollution, especially from waste, is a serious global problem. Using renewable energy like sunlight with photocatalysts offers an environmentally friendly way to remove pollutants. The focus of the innovation is the use of V, Er, and Ce-doped, multilayer mosaic-structured TiO2 thin films coated on glass substrates with their suitable band gap values to enhance the performance and sustainability of traditional TiO2 photocatalysts for the effective treatment of cyanide-containing wastewater under sunlight/UV light. In this study, it was aimed to produce V, Er, Ce pure/doped TiO2 thin coatings on glass substrates with sol–gel technique and photocatalytic degradation of cyanide in wastewater by using these substrates. The structural, microstructural and electrical properties of the produced films were investigated and thin films coated on glass substrates were used as photocatalysts in the photocatalytic degradation of cyanide in wastewater under UV/sun light source. As an innovative approach, laboratory and industrial scale TiO2, V-TiO2, Er-TiO2, and Ce-TiO2 coatings with the anatase phase on glass substrates exhibit a multilayered mosaic architecture. The coatings’ refractive index, film thickness, and energy bandgap were observed to vary within the ranges of 1.6028–1.6075 nD, 2.408–2.750 μm, and 3.08–3.73 eV, respectively. Notably, a 95 % efficiency was achieved in cyanide degradation from wastewater using these modified TiO2 films, indicating their significant potential for high-performance photocatalytic applications in environmental remediation. Photocatalytic samples demonstrated effective cyanide degradation over 10 industrial-scale cycles, with efficiency declining due to impurity buildup from real wastewater. Cleaning the surface restored activity, highlighting the material’s potential for recyclability. As a result, this innovation offers up to 95 % cyanide removal efficiency, reusability and sustainability through surface cleaning, and applicability at industrial scale.
工业、农业和家用化学品日益污染环境,即使浓度很低也会影响水、空气和土壤。这种污染,特别是来自废物的污染,是一个严重的全球性问题。使用可再生能源,如阳光和光催化剂,提供了一种环保的方式来去除污染物。创新的重点是使用V, Er和ce掺杂的多层马赛克结构TiO2薄膜涂覆在合适的带隙值的玻璃基板上,以提高传统TiO2光催化剂的性能和可持续性,从而在日光/紫外光下有效处理含氰废水。本研究旨在利用溶胶-凝胶技术在玻璃基板上制备V, Er, Ce纯/掺杂TiO2薄膜,并利用这些基板光催化降解废水中的氰化物。研究了所制备薄膜的结构、微观结构和电学性能,并将其涂覆在玻璃基板上作为光催化剂,在紫外/太阳光源下光催化降解废水中的氰化物。作为一种创新的方法,实验室和工业规模的TiO2, V-TiO2, Er-TiO2和Ce-TiO2涂层具有锐钛矿相在玻璃基板上呈现多层马赛克结构。涂层的折射率、膜厚和能带分别在1.6028 ~ 1.6075 nD、2.408 ~ 2.750 μm和3.08 ~ 3.73 eV范围内变化。值得注意的是,使用这些改性TiO2薄膜降解废水氰化物的效率达到95%,这表明它们在环境修复中的高性能光催化应用潜力巨大。光催化样品在10个工业规模循环中证明了有效的氰化物降解,由于实际废水中的杂质堆积,效率下降。清洁表面恢复了活性,突出了材料的可回收性潜力。因此,这一创新提供了高达95%的氰化物去除效率,通过表面清洁可重复使用和可持续性,并具有工业规模的适用性。
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引用次数: 0
Novel Z-scheme BiOCl/g-C3N4 nanocomposite for high performance photocatalytic degradation of organic pollutants and charge carrier dynamics 新型Z-scheme BiOCl/g-C3N4纳米复合材料的高效光催化降解有机污染物及载流子动力学研究
Q1 Environmental Science Pub Date : 2025-06-20 DOI: 10.1016/j.enmm.2025.101086
Orawan Rojviroon , Gomathi Abimannan , Priyadharsan Arumugam , Maadeswaran Palanisamy , Ranjith Rajendran , Govarthini Ramasamy , Sanya Sirivithayapakorn , Natacha Phetyim , Thammasak Rojviroon
In this research work, Z scheme BiOCl/g-C3N4 nanocomposite was synthesized through hydrothermal process and combined with thermal decomposition method. Numerous characterization techniques were utilized to examine the phase structure, functional groups, morphology, elemental composition, electronic structure and optical behaviour of as synthesized materials. The boosted light absorption capability of BiOCl/g-C3N4 nanocomposite which is accredited to the synergetic interaction between the BiOCl and g-C3N4 materials. The photocatalytic degradation efficacy of BiOCl/g-C3N4 nanocomposite over Rhodamine B (RhB) textile pollutant was exhibited 97 % within 100 min which is higher than the pristine BiOCl material. It’s caused by the active separation, allocation of electrons and holes and reduce the recombination. Five successive recycle process proved the stability and reusability of the material. Finally, This work demonstrates an enriched Z scheme BiOCl/g-C3N4 nanocomposite will deliver the impression of construct the Z scheme heterojunction photocatalyst to augment the photocatalytic activity in the occurrence of visible light.
本研究采用水热法结合热分解法合成了Z型BiOCl/g-C3N4纳米复合材料。许多表征技术被用于检测合成材料的相结构、官能团、形态、元素组成、电子结构和光学行为。BiOCl/g-C3N4纳米复合材料的光吸收能力增强是由于BiOCl和g-C3N4材料之间的协同作用。在100 min内,BiOCl/g-C3N4纳米复合材料对罗丹明B (Rhodamine B, RhB)纺织污染物的光催化降解效率达到97%,高于原始BiOCl材料。它是由电子和空穴的主动分离、分配和减少复合引起的。连续五次的回收过程证明了材料的稳定性和可重复使用性。最后,本研究证明了富含Z方案的BiOCl/g-C3N4纳米复合材料将提供构建Z方案异质结光催化剂的效果,以增强可见光发生时的光催化活性。
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引用次数: 0
Quantifying silver and gold nanoparticles in water via carbazole fluorescence quenching: A simple and economical approach 通过咔唑荧光猝灭定量水中的银和金纳米粒子:一种简单而经济的方法
Q1 Environmental Science Pub Date : 2025-06-14 DOI: 10.1016/j.enmm.2025.101084
Rodrigo Nicolás Núñez , Alicia Viviana Veglia , Natalia Lorena Pacioni
The fluorescence quenching of carbazole and carbazole@2-hydroxypropyl-β-cyclodextrin complex was evaluated in water as an analytical strategy for the quantification of six different silver and gold nanoparticles with either gallic acid, citrate, or p-(2-hydroxyethoxy) benzoic acid as ligands. The free carbazole is more sensitive to the analyzed metal nanoparticles with detection limits in the picomolar level (e.g., 0.106 pM for citrate-stabilized silver nanorods (AgNR) and 34.5 pM for citrate-stabilized silver nanospheres (AgNPc)) compared to the cyclodextrin-complexed carbazole (e.g., 0.200 pM for AgNR to insensitive for AgNPc). The recovery assays in spiked tap water and surface river water for all the analyzed nanoparticles were between 90 % and 112 % with 95 % confidence. The proposed method is an excellent alternative to more sophisticated methodologies for accurately quantifying silver and gold nanoparticles in aqueous systems.
以没食子酸、柠檬酸或对(2-羟基乙氧基)苯甲酸为配体,评价了咔唑和carbazole@2-hydroxypropyl-β-环糊精配合物在水中的荧光猝灭,作为对六种不同银和金纳米粒子的定量分析策略。游离卡唑对所分析的金属纳米颗粒更敏感,检测限在皮摩尔水平(例如,柠檬酸稳定的银纳米棒(AgNR)为0.106 pM,柠檬酸稳定的银纳米球(AgNPc)为34.5 pM),而环dextrin配合的卡唑(例如,AgNR为0.200 pM,对AgNPc不敏感)。在自来水和地表水中的回收率为90% ~ 112%,置信度为95%。所提出的方法是一个很好的替代更复杂的方法,准确定量在水系统中的银和金纳米颗粒。
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引用次数: 0
Green synthesis of Nigella sativa-mediated silver nanoparticles for enhanced antibacterial activity and wound healing: Mechanistic insights and biomedical applications 绿色合成黑草介导的银纳米颗粒增强抗菌活性和伤口愈合:机理见解和生物医学应用
Q1 Environmental Science Pub Date : 2025-06-12 DOI: 10.1016/j.enmm.2025.101085
Chella Perumal Palanisamy , Sirilux Poompradub , Kanokwan Sansanaphongpricha , Selvaraj Jayaraman , Karthik Subramani , Faridah Sonsudin
This study demonstrates an eco-friendly synthesis of silver nanoparticles (AgNPs) using chloroform extract of Nigella sativa seeds (CENSS) for combating bacterial infections and accelerating wound repair. The work highlights the dual therapeutic potential of CENSS-AgNPs through rigorous physicochemical, biological, and mechanistic analyses. The stable AgNPs was formed because of the transformation of silver ions by the CENSS. These NPs were thoroughly characterized using various physiochemical parameters. The biosynthesized CENSS-AgNPs demonstrated substantial antibacterial activity as indicated by the prominent inhibition areas observed on the agar plates. These are prominent bacteria which play significant roles in both human health and disease. Cytotoxicity assessment on human keratinocyte cells (HaCaT) revealed dose-dependent effects, with CENSS-AgNPs demonstrating feasible in wound healing by hastening scratch closure and enhancing cell migration. Furthermore, the protein expression analysis explored that CENSS-AgNPs stimulated the expression levels of platelet-derived growth factor (PDGF) and vascular endothelial growth factor (VEGF) which are crucial for wound repair. Over all, this study underscores the therapeutic promise of CENSS-mediated AgNPs in combating infections and promoting tissue regeneration, suggesting their prospective utility in advanced wound care and biomedical fields. Further exploration of their biological mechanisms and clinical applications is warranted to harness their full therapeutic potential.
这项研究展示了一种生态友好的合成银纳米粒子(AgNPs)的方法,该方法使用Nigella sativa种子(CENSS)的氯仿提取物来对抗细菌感染和加速伤口修复。通过严格的物理化学、生物学和机制分析,这项工作强调了CENSS-AgNPs的双重治疗潜力。稳定的AgNPs是由CENSS对银离子的转化而形成的。利用各种理化参数对这些NPs进行了全面表征。生物合成的CENSS-AgNPs显示出显著的抗菌活性,这表明在琼脂板上观察到明显的抑制区。这些都是在人类健康和疾病中发挥重要作用的重要细菌。对人角质形成细胞(HaCaT)的细胞毒性评估显示出剂量依赖效应,CENSS-AgNPs通过加速划痕闭合和增强细胞迁移,在伤口愈合中证明是可行的。此外,蛋白质表达分析发现,CENSS-AgNPs刺激了血小板衍生生长因子(PDGF)和血管内皮生长因子(VEGF)的表达水平,这对伤口修复至关重要。总之,这项研究强调了cnss介导的AgNPs在对抗感染和促进组织再生方面的治疗前景,表明它们在高级伤口护理和生物医学领域的潜在应用。进一步探索其生物学机制和临床应用是必要的,以充分利用其治疗潜力。
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引用次数: 0
rGO/Carbon composite-based electrocatalytic electrodes for efficient nitrate adsorption and reduction − current challenges and future perspective 基于氧化石墨烯/碳复合材料的高效硝酸盐吸附和还原电催化电极-当前挑战和未来展望
Q1 Environmental Science Pub Date : 2025-06-01 DOI: 10.1016/j.enmm.2025.101080
Krishnan Vancheeswaran Prasad , Rachel Angeline Lenin , Mohanraj Kumar , Jih-Hsing Chang
The summary of this review paper addresses the pressing issue of nitrate contamination in water sources, increasing concern primarily due to agricultural runoff and industrial waste. Elevated nitrate levels pose significant risks to both human health, such as methemoglobinemia (blue baby syndrome), and aquatic ecosystems through processes like eutrophication. The paper examines the potential of carbon composite-based electrocatalytic electrodes, particularly those incorporating reduced graphene oxide (rGO), for effectively removing nitrates from contaminated water. The review uniquely contributes by analyzing nitrate reduction mechanisms, rGO’s catalytic role, electrode fabrication challenges, operational stability, pilot-scale implementation, and pathways for industrial adoption of rGO-based electrocatalysts. The high surface area of these materials makes them interesting, have superior conductivity, and excellent catalytic properties, which enhance their ability to adsorb and reduce nitrate ions. It demonstrates how major advancements in carbon composites have improved the effectiveness and selectivity of nitrate reduction, demonstrating their potential for real-world applications. However, challenges remain, particularly about scalability, the durability of the materials, and the unwanted production of by-products like ammonia during the reduction process. The further research is necessary to overcome these challenges by focusing on the development of more stable, scalable, and cost-effective materials. Reducing harmful by-products will also be essential for practical industrial applications. Advancements in this field will contribute to sustainable water treatment and the achievement of Sustainable Development Goal, which focuses on clean water and sanitation.
本文综述了水源中硝酸盐污染的紧迫问题,主要是由于农业径流和工业废水引起的。硝酸盐水平升高对人类健康(如高铁血红蛋白血症(蓝婴综合症))和水生生态系统(如富营养化)都构成重大风险。本文研究了基于碳复合材料的电催化电极的潜力,特别是那些含有还原氧化石墨烯(rGO)的电极,可以有效地去除污染水中的硝酸盐。该综述通过分析硝酸还原机制、氧化石墨烯的催化作用、电极制造挑战、操作稳定性、中试规模实施以及工业采用氧化石墨烯电催化剂的途径,做出了独特的贡献。这些材料的高表面积使它们变得有趣,具有优异的导电性和优异的催化性能,这增强了它们吸附和还原硝酸盐离子的能力。它展示了碳复合材料的重大进步如何提高了硝酸盐还原的有效性和选择性,展示了它们在现实世界中的应用潜力。然而,挑战依然存在,特别是在可扩展性、材料的耐久性以及在还原过程中产生的副产品(如氨)方面。为了克服这些挑战,进一步的研究是必要的,重点是开发更稳定、可扩展和更具成本效益的材料。减少有害的副产品对实际工业应用也至关重要。这一领域的进展将有助于可持续水处理和实现以清洁水和卫生为重点的可持续发展目标。
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引用次数: 0
Antimony retention and transformation: a novel approach using microfluidics and hydrogel, biocomposite nanomagnetite aggregates 锑的保留和转化:一种利用微流体和水凝胶、生物复合纳米磁铁矿聚集体的新方法
Q1 Environmental Science Pub Date : 2025-06-01 DOI: 10.1016/j.enmm.2025.101083
Evgenia-Maria Papaslioti , Hervé Tabuteau , Julien Farasin , Delphine Vantelon , Valerie Magnin , Laurent Charlet
Antimony (Sb) is a redox sensitive metalloid increasingly recognized as an emerging contaminant of global concern due to its toxicity and widespread occurrence in natural and anthropogenically impacted water systems. It is commonly found in both drinking and wastewater, where it poses potential risks to human health. Magnetite nanoparticles, known as active retention agents for redox-sensitive contaminants, are combined here with polymeric matrices to ease their application in water treatment systems and to enhance their stability, dispersibility, and sorption efficiency. In this study, we assess Sb retention using hydrogel-nanomagnetite aggregates, with and without chitosan coating, under flow-through microfluidic conditions that mimic natural and engineered aquatic environments. Advanced synchrotron-based μ-XRF mapping and μ-XANES spectroscopy were employed for the first time to such integrated system to simultaneously resolve the spatial distribution and oxidation state of sorbed Sb. Antimonate immobilization followed two distinct, input concentration-dependent pathways: (i) reduction to Sb(III), forming stable inner-sphere Fe–O–Sb complexes, or (ii) adsorption via electrostatic and complexation mechanisms. At low Sb(V) concentrations reduction is favored in chitosan-free aggregates, enabling homogeneous Sb(III) diffusion through the media. At higher concentrations, and particularly in chitosan-coated systems, Sb(V) is immobilized predominantly via adsorption, accumulating on the rim of the aggregates. Chitosan enhances Sb(V) sorption by providing positively charged functional groups and, along with pH and Sb input concentration, controls Sb sorption processes. These findings deepen the understanding of Sb retention mechanisms through redox and sorption interactions in polymer-supported magnetite systems, as revealed using microfluidics technology, and provide a new foundation for the development of advanced water treatment technologies with international relevance for mitigating redox-sensitive contaminants.
锑(Sb)是一种氧化还原敏感类金属,由于其毒性和广泛存在于自然和人为影响的水系统中,越来越被认为是全球关注的新兴污染物。它通常存在于饮用水和废水中,对人类健康构成潜在风险。磁性纳米颗粒,被称为氧化还原敏感污染物的活性保留剂,在这里与聚合物基质结合,以减轻其在水处理系统中的应用,并提高其稳定性,分散性和吸附效率。在这项研究中,我们使用水凝胶-纳米磁铁矿聚集体,在模拟自然和工程水生环境的流过微流控条件下,在有壳聚糖涂层和没有壳聚糖涂层的情况下,评估了Sb的保留率。基于同步加速器的μ-XRF图谱和μ-XANES光谱首次应用于该集成系统,同时解析了吸附Sb的空间分布和氧化状态。锑酸盐固定化遵循两种不同的输入浓度依赖途径:(i)还原Sb(III),形成稳定的球内Fe-O-Sb配合物,或(ii)通过静电和络合机制吸附Sb。在低Sb(V)浓度下,无壳聚糖的聚集体有利于还原,使Sb(III)在介质中均匀扩散。在较高浓度下,特别是在壳聚糖包覆体系中,Sb(V)主要通过吸附固定,积聚在聚集体的边缘。壳聚糖通过提供带正电荷的官能团增强Sb(V)的吸附,并与pH和Sb输入浓度一起控制Sb的吸附过程。这些发现加深了对聚合物支撑的磁铁矿系统中通过氧化还原和吸附相互作用的Sb保留机制的理解,并为开发具有国际相关性的先进水处理技术提供了新的基础,以减轻氧化还原敏感污染物。
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引用次数: 0
Novel insights into the presence and risks of phthalate esters in the Citarum River, Indonesia: Seasonal variations 新见解的存在和邻苯二甲酸酯的风险在Citarum河,印度尼西亚:季节性变化
Q1 Environmental Science Pub Date : 2025-06-01 DOI: 10.1016/j.enmm.2025.101082
Diana Rahayuning Wulan , Nurul Fahimah , Mariska Margaret Pitoi , Raden Tina Rosmalina , Muammar Qadafi , Hanny Meirinawati , Wulan Ayu Ningsih
This study investigates the occurrence and risks of phthalate acid esters (PAEs) in the Citarum River across 11 sampling sites during rainy and dry seasons. The average total concentration of PAEs was higher in the rainy season (79.18 ± 50.51 µg/L) than in the dry season (1.67 ± 0.71 µg/L). Dimethyl phthalate (DMP), diethyl phthalate (DEP), and bis (2-Ethylhexyl) phthalate (DEHP) were detected only during the rainy season with concentration ranges of not detected (ND) - 7.284, 7.135 - 55.674, and ND - 20.713 µg/L, respectively. Dibutyl phthalate (DBP) was present in both seasons, with an increase from ND - 2.758 µg/L (dry season) to 9.681 - 160.245 µg/L (rainy season), contributing to elevated levels of endocrine-disrupting chemicals (EDCs) (Estradiol Equivalent Concentration (EEQ) > 0.002 µg/L). Ecological risks were low during the dry season but rose to high levels in the rainy season (risk quotient (RQ) > 1), driven by DBP and DEP exposure. Health risk assessments showed non-carcinogenic risks (target hazard quotient (THQ) < 1) for consuming Tilapia sp. and Common carp at most sites, except one upstream location during the rainy season, where toddlers were at risk. DBP was the main contributor to these risks, accounting for 80.85% in Tilapia sp. and 89.05% in Common carp. DEHP-associated cancer risks were absent in the dry season but appeared at one location during the rainy season. The findings highlight the urgent need to address PAEs pollution in the Citarum River through source control, monitoring in water compartments, and establishing regulatory limits for PAEs in wastewater and surface waters.
本研究调查了Citarum河在雨季和旱季11个采样点中邻苯二甲酸酯(PAEs)的发生和风险。雨季PAEs平均总浓度(79.18±50.51µg/L)高于旱季(1.67±0.71µg/L)。邻苯二甲酸二甲酯(DMP)、邻苯二甲酸二乙酯(DEP)和邻苯二甲酸二乙酯(DEHP)仅在雨季检测到,浓度范围分别为未检出(ND) - 7.284、7.135 - 55.674和ND - 20.713µg/L。两个季节都存在邻苯二甲酸二丁酯(DBP),从ND - 2.758µg/L(旱季)增加到9.681 - 160.245µg/L(雨季),导致内分泌干扰化学物质(EDCs)水平升高(雌二醇当量浓度(EEQ) >;0.002µg / L)。旱季生态风险较低,雨季生态风险较高(RQ) >;1) DBP和DEP暴露驱动。健康风险评估显示非致癌风险(目标危害商(THQ) <;1)在大多数地点食用罗非鱼和鲤鱼,除了一个上游地点在雨季,幼儿有危险。DBP是这些风险的主要贡献者,在罗非鱼中占80.85%,在鲤鱼中占89.05%。dehp相关的癌症风险在旱季不存在,但在雨季出现在一个地点。研究结果强调了解决Citarum河中PAEs污染的迫切需要,包括通过源头控制、水区监测以及建立废水和地表水中PAEs的监管限制。
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引用次数: 0
Cobalt iron oxide nanorods with multi functions: solvothermal synthesis and characterizations as potent antimicrobial agent and photocatalyst 多功能氧化钴铁纳米棒:溶剂热合成及其抗菌和光催化剂的表征
Q1 Environmental Science Pub Date : 2025-06-01 DOI: 10.1016/j.enmm.2025.101079
Bushra Uzair , Zukhra Abbasi , Basma Gul , Zulqurnain Ali , Khuram Shahzad , Sadaf Mushtaq , Farid Menaa
The escalating concerns over microbial infections and environmental pollution necessitate the exploration of advanced materials that can effectively address both issues. In this research paper, the microwave-assisted solvothermal method was used to synthesize multifunctional hybrid materials based on cobalt-iron oxide (CoFe2O4) nanorods. X-ray diffraction (XRD), Fourier-Transform Infrared Spectroscopy (FT-IR), and Scanning Electron Microscopy (SEM) analyze the physicochemical properties of the nanomaterial. SEM analysis revealed rod-shaped crystals with an average particle size of 40 nm, while XRD confirmed crystalline nature of cobalt-iron oxide nanoparticles (CIO NRs). The prepared CIO nanorods showed promising antibacterial activity (p < 0.0001) against MDR Pseudomonas aeruginosa, exhibiting a notable zone of inhibition measuring 25 mm. Furthermore, they displayed significant (p < 0.001) antifungal properties inhibiting the growth of Aspergillus flavus (18 mm), Aspergillus niger (23 mm) and Candida albicans (25 mm). Moreover, the CoFe2O4 nanorods inhibited 90 % biofilm formation by Pseudomonas aeruginosa on human teeth, highlighting their potential utility in clinical contexts. Furthermore, CoFe2O4 NRs demonstrated significant efficacy in degrading methylene blue (MB) 96 %, malachite green (MG) 95 %, and methyl orange (MO) 98 % dyes under sunlight irradiation conditions. Together, these findings emphasize the versatility of CIONRs that could add significant value to their applicability in medicine as a solution for diverse microbial infections and water treatment technologies.
对微生物感染和环境污染的日益关注要求探索能够有效解决这两个问题的先进材料。本文采用微波辅助溶剂热法制备了基于钴氧化铁纳米棒的多功能杂化材料。x射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)和扫描电子显微镜(SEM)分析了纳米材料的物理化学性质。SEM分析显示,纳米钴氧化铁颗粒的平均粒径为40 nm, XRD分析证实了纳米钴氧化铁颗粒(CIO NRs)的结晶性质。制备的CIO纳米棒具有良好的抗菌活性(p <;0.0001)抗耐多药铜绿假单胞菌,表现出25 mm的显著抑制区。此外,他们表现出显著的(p <;0.001)抗真菌特性,抑制黄曲霉(18 mm)、黑曲霉(23 mm)和白色念珠菌(25 mm)的生长。此外,CoFe2O4纳米棒抑制了90%铜绿假单胞菌在人牙齿上形成的生物膜,突出了其在临床中的潜在用途。此外,在日光照射条件下,CoFe2O4 NRs对亚甲基蓝(MB)、孔雀石绿(MG)和甲基橙(MO)的降解率分别为96%、95%和98%。总之,这些发现强调了cionr的多功能性,可以为其在医学上的适用性增加重要价值,作为各种微生物感染和水处理技术的解决方案。
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引用次数: 0
Environmentally friendly synthesis of gold nanoparticles at room temperature for chlorpyrifos-methyl detection in water samples 室温下环境友好合成金纳米颗粒用于水样中甲基毒死蜱的检测
Q1 Environmental Science Pub Date : 2025-05-23 DOI: 10.1016/j.enmm.2025.101081
Ángela Yanina Aguilera , Yasmin Safe , Sára Doubravská , Valeria Springer
In this study, a facile synthesis of gold nanoparticles (AuNPs) is achieved through an environmentally friendly method in less than 2 min, using ascorbic acid and pentetic acid as reducing and stabilizing agents, under alkaline conditions at room temperature. The effects of the main experimental parameters on the synthesis performance were analyzed using response surface methodology. The obtained particles, spherical in shape and with average size of 9.2 nm, were tested as sensor for determination of chlorpyrifos-methyl (CPM), an organophosphate insecticide widely used in agriculture practices and households, which represent a major concern for the environment and human health. CPM was determined through the changes on the localized surface plasmon resonance (LSPR) band of AuNPs at 527 nm. Under optimal conditions, the method was evaluated in the concentration range between 5.00 and 40.0 μg L-1, with R2 > 0.98, limit of detection of 3.79 µg L-1 and RSD values lower than 6.5 %. The applicability of this methodology for the analysis of real samples, including river water and well water, was tested with satisfactory recovery values (84.0–––98.8 %). Besides, the practicality and functionality of the proposed method were assessed by the Blue Applicability Grade Index (BAGI), a new metric tool developed in 2023, with an outstanding performance.
在本研究中,采用抗坏血酸和戊酸作为还原剂和稳定剂,在室温碱性条件下,通过一种环保的方法,在不到2分钟的时间内实现了金纳米颗粒(AuNPs)的快速合成。利用响应面法分析了主要实验参数对合成性能的影响。所获得的颗粒呈球形,平均大小为9.2纳米,作为测定甲基毒死蜱(CPM)的传感器进行了测试。CPM是一种广泛用于农业实践和家庭的有机磷杀虫剂,对环境和人类健康构成重大关切。通过AuNPs在527 nm处局部表面等离子体共振(LSPR)带的变化来确定CPM。在最佳条件下,该方法在5.00 ~ 40.0 μg -1的浓度范围内进行评价,R2 >;0.98,检出限为3.79µg L-1, RSD值小于6.5%。该方法适用于实际样品的分析,包括河水和井水,回收率(84.0—98.8%)令人满意。此外,该方法的实用性和功能性在2023年开发的新度量工具蓝色适用性等级指数(BAGI)中得到了突出的评价。
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引用次数: 0
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Environmental Nanotechnology, Monitoring and Management
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