Removal efficiency

去除效率
  • 文章类型: Journal Article
    电动修复(EKR)在修复原位污染土壤方面显示出巨大的潜力。对于含水率高、渗透性低的重金属污染软粘土,使用将电解质放置在地面上方的电动修复方法来避免诸如电解质泄漏和可能由于将电解质直接注入土壤而引起的二次污染的问题。在这种情况下,使用这种新颖的实验装置,进行了一组柠檬酸(CA)增强的EKR试验,以研究Cu和Zn污染的软粘土的最佳设计参数。这些测试中重金属Cu和Zn的平均去除率在27.9-85.5%和63.9-83.5%之间,分别。结果表明,锌的去除是有效的。这是由电渗流的迁移强度决定的,特别是阳极电解液的体积减少。影响铜去除效率的主要因素依次为污染软黏土的有效电位和电解液浓度。基于这些参数设计实验参数将有助于去除Cu和Zn。此外,污染土壤的抗剪强度得到了提高;然而,改善程度有限。低浓度CA能有效控制阳极与土壤的接触电阻,阴极和土壤之间的接触电阻,通过增加电解质的量和电解质与土壤之间的接触面积来提高土壤电阻。
    Electrokinetic remediation (EKR) has shown great potential for the remediation of in situ contaminated soils. For heavy metal-contaminated soft clay with high moisture content and low permeability, an electrokinetic remediation method with electrolytes placed above the ground surface is used to avoid issues such as electrolyte leakage and secondary contamination that may arise from directly injecting electrolytes into the soil. In this context, using this novel experimental device, a set of citric acid (CA)-enhanced EKR tests were conducted to investigate the optimal design parameters for Cu- and Zn-contaminated soft clay. The average removal rates of heavy metals Cu and Zn in these tests were in the range of 27.9-85.5% and 63.9-83.5%, respectively. The results indicate that the Zn removal was efficient. This was determined by the migration intensity of the electro-osmotic flow, particularly the volume reduction of the anolyte. The main factors affecting the Cu removal efficiency in sequence were the effective electric potential of the contaminated soft clay and the electrolyte concentration. Designing experimental parameters based on these parameters will help remove Cu and Zn. Moreover, the shear strength of the contaminated soil was improved; however, the degree of improvement was limited. Low-concentration CA can effectively control the contact resistance between the anode and soil, the contact resistance between the cathode and soil, and the soil resistance by increasing the amount of electrolyte and the contact area between the electrolyte and soil.
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  • 文章类型: Journal Article
    水中的全氟烷基和多氟烷基物质(PFAS)由于其极端的化学稳定性和潜在的健康风险而需要充分去除。膜分离可以是一个有前途的策略,而用于PFAS去除的具有常规结构的膜通常面临诸如有限的效率和稳定性等挑战。在这项研究中,通过在具有MOF纳米片的层状膜的构建过程中引入界面聚合过程,开发了一种具有聚酰胺(PA)局部改性的新型金属有机框架(MOF)膜。得益于致密的结构和强大的负表面电荷,PA修饰的MOF膜可以有效去除11种PFAS(分子量为214.0至514.1Da的5种短链和6种长链),特别是对短链PFAS的高拒绝(超过84%),伴随着显著的透水量21.4L·m²·h-bar-1。通过阐明各种排斥机制,深入分析了PFAS的膜去除特性,具有特别区别的排斥和吸附能力。此外,膜稳定性明显增强,超声处理10分钟后的结构完整性和连续过滤120小时的稳定分离效率证明。具有增强的表面亲水性和负电荷以及致密的膜孔,与传统的层状和PA膜相比,新型膜还表现出更优异的抗污染性能,进一步体现了实际应用的优势。这项工作为开发专门用于高效去除PFAS的高性能膜提供了一个有前途的解决方案。解决水处理的关键需求。
    Per- and polyfluoroalkyl substances (PFAS) in water requires sufficient removal due to their extreme chemical stability and potential health risk. Membrane separation can be a promising strategy, while membranes with conventional structures used for PFAS removal often face challenges such as limited efficiency and stability. In this study, a novel metal-organic framework (MOF) membrane with local modification of polyamide (PA) was developed by introducing interfacial polymerization process during the construction of lamellar membranes with MOF nanosheets. Benefiting from the dense structure and strong negative surface charge, the PA-modified MOF membrane could effectively remove 11 types of PFAS (five short-chain and six long-chain ones with molecular weights ranging from 214.0 to 514.1 Da), especially displaying high rejections for short-chain PFAS (over 84%), along with a remarkable water permeance of 21.4 L·m⁻²·h⁻¹·bar⁻1. The membrane removal characteristics for PFAS were deeply analyzed by elucidating various rejection mechanisms, with particularly distinguishing the rejection and adsorption capacity. Moreover, the membrane stability was significantly enhanced, demonstrated by the structural integrity after 10 min of ultrasonic treatment and stable separation efficiency over 120 h of continuous filtration. With enhanced surface hydrophilicity and negative charge as well as dense membrane pores, the novel membrane also exhibited more superior anti-fouling performance compared to conventional lamellar and PA membranes, further manifesting advantages for practical applications. This work provides a promising solution for developing high-performance membranes tailored specifically for efficient PFAS removal, addressing a critical need in water treatment.
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  • 文章类型: Journal Article
    在这项研究中,使用Raoultellasp.构建了微生物燃料电池。XY-1有效降解四环素(TC)并评估电化学系统的有效性。7天期间降解率达到83.2±1.8%,其中系统含有30毫克/升的TC,并鉴定了降解途径和中间体。低浓度的TC增强阳极生物膜发电,而高浓度的TC降低了生物膜的电化学活性,胞外聚合物,和与电子转移相关的酶活性。引入产电细菌提高了发电效率。使用Castellaniellasp。制造了三菌株混合系统。A3,Castellaniellasp。A5和Raoultellasp.XY-1,导致90.4%的TC降解率增强,最大输出电压从200增加到265mV。本研究提出了一种利用四环素降解菌作为生物阳极去除TC的策略,同时掺入产电细菌以增强发电量。
    In this study, a microbial fuel cell was constructed using Raoultella sp. XY-1 to efficiently degrade tetracycline (TC) and assess the effectiveness of the electrochemical system. The degradation rate reached 83.2 ± 1.8 % during the 7-day period, in which the system contained 30 mg/L TC, and the degradation pathway and intermediates were identified. Low concentrations of TC enhanced anodic biofilm power production, while high concentrations of TC decreased the electrochemical activity of the biofilm, extracellular polymeric substances, and enzymatic activities associated with electron transfer. Introducing electrogenic bacteria improved power generation efficiency. A three-strain hybrid system was fabricated using Castellaniella sp. A3, Castellaniella sp. A5 and Raoultella sp. XY-1, leading to the enhanced TC degradation rate of 90.4 % and the increased maximum output voltage from 200 to 265 mV. This study presents a strategy utilizing tetracycline-degrading bacteria as bioanodes for TC removal, while incorporating electrogenic bacteria to enhance electricity generation.
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  • 文章类型: Journal Article
    新兴污染物(EP)在全球水生环境中普遍存在。研究人员努力在将它们释放到环境中之前了解它们的发生和行为。在这项研究中,我们检查了五个污水处理厂(WWTP),收集50个废水样品和10个污泥样品。我们使用质量平衡方程探索了这些WWTP中邻苯二甲酸酯(PAEs)的来源和目的地。废水处理降低了PAEs的频率和浓度,并降低了短链PAEs的比例。我们证实了初级治疗后PAEs浓度的增加,并修改了质量平衡方程。计算表明,冬季比夏季弱的“混合”和冬季比夏季强的沉降导致冬季废水处理对PAEs的去除效率很高。生物降解的质量通量受生物降解效率和收集的特定类型PAEs强度的组合影响,没有季节性差异。污泥沉降的质量通量主要受季节影响,冬季高于夏季。这项研究增强了我们对手动处理设施中新兴污染物的了解,并为优化水专业人员的废水处理方法提供了见解。
    Emerging pollutants (EPs) are prevalent in aquatic environments globally. Researchers strive to understand their occurrence and behavior prior to their release into the environment. In this study, we examined five wastewater treatment plants (WWTPs), collected 50 wastewater samples and 10 sludge samples. We explored the sources and destinations of phthalic acid esters (PAEs) within these WWTPs using mass balance equations. Wastewater treatment diminished the frequency and concentration of PAEs, and decreased the fraction of short-chain PAEs. We confirmed the increased concentration of PAEs post-primary treatment and modified the mass balance equation. Calculations suggest that weaker \"the mix\" in winter than in summer and stronger sedimentation in winter than in summer resulted in high efficiency of PAEs removal by winter wastewater treatment. The mass flux of biodegradation was influenced by the combination of biodegradation efficiency and the strength of the particular type of PAEs collected, with no seasonal differences. Mass fluxes for sludge sedimentation were mainly influenced by season and were higher in winter than in summer. This study enhances our understanding of emerging pollutants in manual treatment facilities and offers insights for optimizing wastewater treatment methods for water professionals.
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  • 文章类型: Journal Article
    微生物诱导碳酸盐沉淀(MICP),作为一种环保且有前途的技术,可以将游离金属离子转化为稳定的降水,已被广泛用于重金属污染的修复。然而,由于重金属毒性对细菌活性的抑制作用,其重金属消除效率下降仍存在问题。在这项工作中,一个高效的,提出了通过将MICP与壳聚糖生物聚合物偶联作为添加剂以减少处理时间的低成本锰(Mn)消除策略,优化,并实施。不同浓度(0.01、0.05、0.10、0.15和0.30%,w/v)对细菌生长的影响,酶活性,研究了所得沉淀的Mn去除效率和微观结构性能。结果表明,通过吸附和生物矿化为MnCO3(初始Mn浓度为3mM),添加0.15%壳聚糖,在12小时内Mn含量降低了94.5%,与无壳聚糖系统相比,修复时间减少了三分之二,而最大脲酶活性增加了50%。微观结构分析表明,矿化沉淀物为球形MnCO3,通过调节壳聚糖中丰富的氨基和羟基,可以获得更小的尺寸和更均匀的MnCO3分布。这些结果表明,壳聚糖通过为矿物形成提供成核位点并减轻金属离子的毒性,加速了MnCO3的成核并调节了MnCO3的生长。有可能以可持续和有效的方式升级MICP流程。本工作为进一步理解生物矿化调控机制提供了参考,并为MICP技术的生物聚合物强化策略在重金属污染中的应用提供了新的视角。
    Microbially induced carbonate precipitation (MICP), as an eco-friendly and promising technology that can transform free metal ions into stable precipitation, has been extensively used in remediation of heavy metal contamination. However, its depressed efficiency of heavy metal elimination remains in question due to the inhibition effect of heavy metal toxicity on bacterial activity. In this work, an efficient, low-cost manganese (Mn) elimination strategy by coupling MICP with chitosan biopolymer as an additive with reduced treatment time was suggested, optimized, and implemented. The influences of chitosan at different concentrations (0.01, 0.05, 0.10, 0.15 and 0.30 %, w/v) on bacterial growth, enzyme activity, Mn removal efficiency and microstructure properties of the resulting precipitation were investigated. Results showed that Mn content was reduced by 94.5 % within 12 h with 0.15 % chitosan addition through adsorption and biomineralization as MnCO3 (at an initial Mn concentration of 3 mM), demonstrating a two-thirds decrease in remediation time compared to the chitosan-absent system, whereas maximum urease activity increased by ∼50 %. Microstructure analyses indicated that the mineralized precipitates were spherical-shaped MnCO3, and a smaller size and more uniform distribution of MnCO3 is obtained by the regulation of abundant amino and hydroxyl groups in chitosan. These results demonstrate that chitosan accelerates nucleation and tunes the growth of MnCO3 by providing nucleation sites for mineral formation and alleviating the toxicity of metal ions, which has the potential to upgrade MICP process in a sustainable and effective manner. This work provides a reference for further understanding of the biomineralization regulation mechanism, and gives a new perspective into the application of biopolymer-intensified strategies of MICP technology in heavy metal contamination.
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  • 文章类型: Journal Article
    家用和个人护理化学品(HPCCs)是日常产品的重要组成部分,随着它们在全球的使用量不断上升。HPCCs最终排放到市政污水处理厂(WWTP)。然而,芽孢杆菌生物反应器(BBR)过程中HPCCs的行为,包括他们的患病率,命运,和消除机制,保持未充分开发。解决这个差距,我们的研究深入研究了在中国东北一个重要的污水处理厂从BBR过程中收集的样本。我们的结果突出了流入液中线性烷基苯磺酸盐(LAS)的优势,浓度在238至789μg/L之间,远高于其他HPCC浓度,并在随后的处理单元中保持主导地位。使用BBR工艺处理后,废水中HPCCs的浓度降低。对不同处理单元的检查强调了清除了60%以上高浓度HPCCs的沉砂池,而(RBC)罐的性能需要提高。除了紫外线辐射(UV)过滤器,季节性变化对BBR工艺中其他HPCCs的浓度和去除效率影响最小。根据质量平衡分析,HPCC去除的重要机制是生物降解和污泥吸附。此外,对最终流出物中的HPCCs残留物进行环境风险评估引起的欧碳(OCT)关注,表示对周围水生环境的中等风险(0.1 Household and personal care chemicals (HPCCs) constitute a significant component of everyday products, with their global usage on the rise. HPCCs are eventually discharged into municipal wastewater treatment plants (WWTPs). However, the behaviors of HPCCs inside the Bacillus Bioreactor (BBR) process, including their prevalence, fate, and elimination mechanisms, remain underexplored. Addressing this gap, our study delves into samples collected from a BBR process at a significant WWTP in the northeast of China. Our results spotlight the dominance of linear alkylbenzene sulfonates (LASs) in the influent with concentrations ranging between 238 and 789 μg/L, much higher than the other HPCC concentrations, and remained dominant in the subsequent treatment units. After treatment using the BBR process, the concentrations of HPCCs in the effluent were diminished. Examination of different treatment units underscores the grit chamber removed over 60% of higher-concentration HPCCs, while the performance of the (RBC) tank needs to be improved. Except for the ultraviolet radiation (UV)-filters, seasonal variations exert minimal impact on the concentrations and removal efficiencies of other HPCCs in the BBR process. According to the mass balance analysis, the important mechanisms for HPCC removal were biodegradation and sludge adsorption. Also, the octocrylene (OCT) concerns raised by the environmental risk assessment of the HPCCs residuals in the final effluent, indicate a moderate risk to the surrounding aquatic environment (0.1 < RQ < 1), whereas other HPCCs have a lower risk level (RQ < 0.1). Overall, the research offers new perspectives on the fate and elimination mechanisms of HPCCs throughout the BBR process.
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  • 文章类型: Journal Article
    好氧堆肥是处理畜牧业产生的粪便的常用方法,并且可以减少粪便中抗生素抗性基因(ARGs)释放到环境中。在这项研究中,我们从两种不同的猪粪堆肥处理中收集了样品,有和没有头孢噻呋酯(CEF),并确定了ARG,移动遗传元件(MGEs),通过宏基因组测序和细菌群落。研究了CEF对ARGs和MGE细菌群落组成和命运的影响。随着堆肥温度和pH值的升高,粪肥中CEF的浓度迅速下降,降解半衰期为1.12d,好氧堆肥10d后去除率为100%。宏基因组学表明,粪肥中的CEF可能抑制厚壁菌和变形杆菌的生长,从而减少了这两种细菌所承载的一些ARG和MGE,ARG和MGE的变化进一步证实了这一点。进一步的冗余分析表明,pH和温度是影响堆肥过程中去除ARG的关键环境因素。intI1和细菌群落对ARG丰度也有显著影响。这些结果对于通过控制一些关键环境因素和动物使用的抗生素类型来促进从动物粪便中去除一些ARGs具有重要意义。
    Aerobic composting is a common way for the disposal of feces produced in animal husbandry, and can reduce the release of antibiotic resistance genes (ARGs) from feces into the environment. In this study, we collected samples from two distinct treatments of swine manure compost with and without ceftiofur (CEF), and identified the ARGs, mobile genetic elements (MGEs), and bacterial community by metagenomic sequencing. The impacts of CEF on the bacterial community composition and fate of ARGs and MGEs were investigated. With increasing composting temperature and pH, the concentration of CEF in the manure decreased rapidly, with a degradation half-life of 1.12 d and a 100% removal rate after 10 d of aerobic composting. Metagenomics demonstrated that CEF in the manure might inhibit the growth of Firmicutes and Proteobacteria, thereby reducing some ARGs and MGEs hosted by these two bacteria, which was further confirmed by the variations of ARGs and MGEs. A further redundancy analysis suggested that pH and temperature are key environmental factors affecting ARG removal during composting, and intI1 and bacterial communities also have significant influence on ARG abundance. These results are of great significance for promoting the removal of some ARGs from animal manure by controlling some key environmental factors and the type of antibiotics used in animals.
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  • 文章类型: Journal Article
    寻求低成本、环保的微生物燃料电池(MFC)反应器电极催化剂近几十年来受到了广泛的关注。在这项研究中,污泥MFC与生物炭改性阳极(BC-300,BC-400和BC-500)耦合,用于实际的啤酒厂废水处理。生物炭的理化性质在很大程度上取决于热解温度,进一步影响废水的去除效率指标。BC-400MFC被证明是有效的TN和NH4+-N去除,而BC-500MFC实现了对COD和TP的最大去除效率,分别达到97.14%和89.67%。生物炭可以通过提高MFC的电化学性能来促进废水中溶解性有机物(DOM)的降解。BC-400MFC的最大输出电压达到410.24mV,还获得了108.05mW/m2的最大发电量,超过原始MFC(BCC-MFC)4.67倍。高通量测序结果表明,富集的电化学活性菌(EAB)和功能菌(Longilinea,脱衣瘤,和假单胞菌)在BC-MFC中,有助于污染物降解和电子转移。此外,生物炭直接影响废水的电导率,同时改变MFC阳极的微生物群落组成。考虑到污染物去除效率的提高和发电量的增加,本研究结果可为生物炭作为MFC催化剂在啤酒废水处理中的应用提供技术参考。
    Seeking low-cost and eco-friendly electrode catalyst of microbial fuel cell (MFC) reactor has received extensive attention in recent decades. In this study, a sludge MFC was coupled with biochar-modified-anode (BC-300, BC-400, and BC-500) for actual brewery wastewater treatment. The physicochemical properties of biochar largely depended on the pyrolysis temperature, further affecting the removal efficiency of wastewater indicators. BC-400 MFC proved to be efficient for TN and NH4+-N removal, while the maximum removal efficiencies of COD and TP were achieved by BC-500 MFC, reaching respectively 97.14 % and 89.67 %. Biochar could promote the degradation of dissolved organic matter (DOM) in wastewater by increasing the electrochemical performances of MFC. The maximum output voltage of BC-400 MFC reached 410.24 mV, and the maximum electricity generation of 108.05 mW/m2 was also obtained, surpassing the pristine MFC (BCC-MFC) by 4.67 times. High-throughput sequencing results illustrated that the enrichment of electrochemically active bacteria (EAB) and functional bacteria (Longilinea, Denitratisoma, and Pseudomonas) in BC-MFCs, contributed to pollutants degradation and electron transfer. Furthermore, biochar affected directly the electrical conductivity of wastewater, simultaneously changing microbial community composition of MFC anode. Considering both enhanced removal efficiency of pollutants and increased power generation, the results of this study would offer technical reference for the application of biochar as MFC catalyst for brewery wastewater treatment.
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  • 文章类型: Journal Article
    新烟碱类杀虫剂(NEO)作为全球最普遍的一类杀虫剂已得到广泛使用,并且在环境中经常被发现,对生物多样性和人类健康构成潜在风险。从废水处理厂(WWTP)排放的废水是环境近地天体的重要来源。然而,通过处理工艺处理后,追踪污水处理厂不同处理单元中NEO变化的研究仍然有限。因此,这项研究旨在使用不同的处理工艺全面调查两个市政污水处理厂中9个母体近地天体(p-NEO)和5种代谢物的命运。UNITANK进水(出水)中∑NEO的平均浓度,厌氧-缺氧-氧(A2/O),循环活性污泥系统(CASS)工艺为189ng/L(195ng/L),173纳克/升(177纳克/升),和123纳克/升(138纳克/升),分别。恐龙,吡虫啉,噻虫嗪,啶虫脒,和噻虫胺是WWTP中最丰富的p-NEO。常规废水处理工艺对废水中的近地天体去除效果不佳(-4.91%至-12.1%),尤其是大型p-NEO。此外,对各种处理单元中近地天体的行为进行了调查。结果表明,生物降解和污泥吸附是消除NEO的主要机制。缺氧或厌氧处理单元可以提高生物处理过程中近地天体的去除效率。然而,终端处理单元(氯化消毒罐)无法清除大多数近地天体。从WWTP释放到华南珠江接收水域的近地天体的估计总量约为6.90-42.6g/d。这些发现为当前废水处理系统中去除近地天体的不同处理工艺的效率提供了新的见解。
    Neonicotinoid insecticides (NEOs) have gained widespread usage as the most prevalent class of insecticides globally and are frequently detected in the environment, posing potential risks to biodiversity and human health. Wastewater discharged from wastewater treatment plants (WWTPs) is a substantial source of environmental NEOs. However, research tracking NEO variations in different treatment units at the WWTPs after being treated by the treatment processes remains limited. Therefore, this study aimed to comprehensively investigate the fate of nine parent NEOs (p-NEOs) and five metabolites in two municipal WWTPs using distinct treatment processes. The mean concentrations of ∑NEOs in influent (effluent) for the UNITANK, anaerobic-anoxic-oxic (A2/O), and cyclic activated sludge system (CASS) processes were 189 ng/L (195 ng/L), 173 ng/L (177 ng/L), and 123 ng/L (138 ng/L), respectively. Dinotefuran, imidacloprid, thiamethoxam, acetamiprid, and clothianidin were the most abundant p-NEOs in the WWTPs. Conventional wastewater treatment processes were ineffective in removing NEOs from wastewater (-4.91% to -12.1%), particularly major p-NEOs. Moreover, the behavior of the NEOs in various treatment units was investigated. The results showed that biodegradation and sludge adsorption were the primary mechanisms responsible for eliminating NEO. An anoxic or anaerobic treatment unit can improve the removal efficiency of NEOs during biological treatment. However, the terminal treatment unit (chlorination disinfection tank) did not facilitate the removal of most of the NEOs. The estimated total amount of NEOs released from WWTPs to receiving waters in the Pearl River of South China totaled approximately 6.90-42.6 g/d. These findings provide new insights into the efficiency of different treatment processes for removing NEOs in current wastewater treatment systems.
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  • 文章类型: Journal Article
    由于纳米塑料污染通过食物和水的摄入在人体内引起的潜在毒性,纳米塑料污染对公共健康提出了重大的全球关注。因此,去除纳米塑料的紧迫任务,特别是水资源,对于提高食品安全至关重要,开发能够有效去除纳米塑料的环保材料至关重要。在这种情况下,我们建议使用可生物降解的阴离子海藻纤维素纳米纤维(TEMPO介导的海藻纤维素纳米纤维,TCNFs)和阳离子海藻纤维素纳米纤维(季铵化海藻纤维素纳米纤维,QCNFs)用于单污染物和共污染物系统中的纳米塑料去除。在我们模拟实际条件下的实验中,我们发现TCNFs和QCNFs对纳米塑料颗粒的平均去除效率为98.71%。此外,与现有材料相比,TCNF和QCNF表现出更高的吸附能力,可能提供具有成本效益的优势。用哺乳动物细胞进行的毒性评估进一步证实了TCNF和QCNF的生物安全性。这项研究有助于使用食用海藻的科学和理论理解,并为有效的食品安全控制提供有希望的解决方案,成本效益高,和生态友好的方式。
    Nanoplastic pollution poses a significant global concern for public health due to the potential toxicity it induces in the human body through food and water intake. Consequently, the urgent task of removing nanoplastics, especially from water resources, is paramount for enhancing food safety, and developing eco-friendly materials capable of efficiently removing nanoplastics is crucial. In this context, we propose the use of biodegradable anionic seaweed cellulose nanofibers (TEMPO-mediated seaweed cellulose nanofibers, TCNFs) and cationic seaweed cellulose nanofibers (quaternized seaweed cellulose nanofibers, QCNFs) for nanoplastic removal in both single- and copollutant systems. In our experiments under simulated practical conditions, we revealed that TCNFs and QCNFs achieved an average removal efficiency of 98.71% against nanoplastic particles. Moreover, TCNFs and QCNFs exhibited higher adsorption capacities compared to those of existing materials, potentially offering a cost-effective advantage. Toxicity assessments conducted with mammalian cells further confirmed the biosafety of TCNFs and QCNFs. This study contributes to the scientific and theoretical understanding of using edible seaweed as well as offers promising solutions for food safety control in an efficient, cost-effective, and eco-friendly manner.
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