wastewater treatment

废水处理
  • 文章类型: Journal Article
    芬顿和类似芬顿的过程,可以产生高活性物质来降解有机污染物,在废水处理领域得到了广泛的应用。其中,Fenton工艺的化学性质,包括活性氧化剂的性质,所涉及的复杂反应,以及其强烈依赖pH的性能的背后原因,是Fenton和类Fenton工艺在废水处理中应用的基础。然而,关于芬顿过程的机制仍然存在矛盾的观点。例如,在此过程中,对活性氧化剂(羟基自由基或四价铁)的性质达成一致共识仍然具有挑战性。本文综合考察了Fenton过程的机理,包括对活性氧化剂性质的评论辩论,涉及芬顿过程的反应,以及Fenton过程中污染物的pH依赖性降解的背后原因。然后,我们总结了几种促进Fe(II)/Fe(III)循环的策略,通过副反应减少活性氧化剂的竞争性消耗,更换芬顿试剂,从而提高了Fenton工艺的性能。此外,提出了未来的进展,包括对活性氧化剂的高精度识别的需求,以及在Fenton工艺降解污染物过程中利用目标污染物的特性。
    Fenton and Fenton-like processes, which could produce highly reactive species to degrade organic contaminants, have been widely used in the field of wastewater treatment. Therein, the chemistry of Fenton process including the nature of active oxidants, the complicated reactions involved, and the behind reason for its strongly pH-dependent performance, is the basis for the application of Fenton and Fenton-like processes in wastewater treatment. Nevertheless, the conflicting views still exist about the mechanism of the Fenton process. For instance, reaching a unanimous consensus on the nature of active oxidants (hydroxyl radical or tetravalent iron) in this process remains challenging. This review comprehensively examined the mechanism of the Fenton process including the debate on the nature of active oxidants, reactions involved in the Fenton process, and the behind reason for the pH-dependent degradation of contaminants in the Fenton process. Then, we summarized several strategies that promote the Fe(II)/Fe(III) cycle, reduce the competitive consumption of active oxidants by side reactions, and replace the Fenton reagent, thus improving the performance of the Fenton process. Furthermore, advances for the future were proposed including the demand for the high-accuracy identification of active oxidants and taking advantages of the characteristic of target contaminants during the degradation of contaminants by the Fenton process.
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  • 文章类型: Journal Article
    抗生素污染已成为一个日益重要的环境问题,作为一种潜在危险的新兴和顽固的污染物,对人类健康构成威胁。在这项研究中,锰过氧化物酶作为全细胞生物催化剂显示在大肠杆菌的外膜上(E.MncoliP)有望降解抗生素。全细胞生物催化剂的锰过氧化物酶活性为13.88±0.25U/L。采用典型的四环素类抗生素金霉素对其降解过程进行分析。50mg/L的金霉素在18h内通过全细胞生物催化剂有效转化。经过六次重复分批反应,在25°C下储存40天后,全细胞生物催化剂保留了87.2%的初始活性,并保留了超过87.46%的初始酶活性。全细胞生物催化剂可以有效去除制药和畜禽废水中的金霉素。因此,高效的全细胞生物催化剂是降解顽固性抗生素的有效替代品,在治疗环境抗生素污染方面具有潜在的应用价值。
    Antibiotic contamination has become an increasingly important environmental problem as a potentially hazardous emergent and recalcitrant pollutant that poses threats to human health. In this study, manganese peroxidase displayed on the outer membrane of Escherichia coli as a whole-cell biocatalyst (E. coli MnP) was expected to degrade antibiotics. The manganese peroxidase activity of the whole-cell biocatalyst was 13.88 ± 0.25 U/L. The typical tetracycline antibiotic chlortetracycline was used to analyze the degradation process. Chlortetracycline at 50 mg/L was effectively transformed via the whole-cell biocatalyst within 18 h. After six repeated batch reactions, the whole-cell biocatalyst retained 87.2 % of the initial activity and retained over 87.46 % of the initial enzyme activity after storage at 25°C for 40 days. Chlortetracycline could be effectively removed from pharmaceutical and livestock wastewater by the whole-cell biocatalyst. Thus, efficient whole-cell biocatalysts are effective alternatives for degrading recalcitrant antibiotics and have potential applications in treating environmental antibiotic contamination.
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  • 文章类型: Journal Article
    电催化耦合生物滤池(EBF)技术有机地融合了电化学和微生物氧化还原的特点,为有效提高生物处理性能提供思路。在这项研究中,开发了一种EBF系统,用于增强污染水中环己酮的降解。实验结果表明,该系统能有效去除污染水中的环己酮。在最优参数下,环己酮的去除率,TP,NH4+-N和TN为97.61±1.31%,76.31±1.67%,分别为94.14±2.13%和95.87±1.01%。降解动力学研究发现,电解,吸附,而生物降解途径在环己酮的降解中起主要作用。微生物群落分析表明,电压可以影响微生物群落的结构,优势属从Acidovorax(0V)转移到Brevundimonas(0.7V)。此外,Acidovorax,Cupriavidus,Ralstonia,和hydrogenophaga在生物膜中具有很高的丰度,可以有效地代谢环己酮及其中间体,有利于环己酮的去除。总之,该研究可指导高稳定性EBF系统的开发和建设,有望用于含环己酮工业废水的深度处理。
    Electrocatalytic coupled biofilter (EBF) technology organically integrates the characteristics of electrochemistry and microbial redox, providing ideas for effectively improving biological treatment performance. In this study, an EBF system was developed for enhanced degradation of cyclohexanone in contaminated water. Experimental results show that the system can effectively remove cyclohexanone in contaminated water. Under the optimal parameters, the removal rates of cyclohexanone, TP, NH4+-N and TN were 97.61 ± 1.31%, 76.31 ± 1.67%, 94.14 ± 2.13% and 95.87 ± 1.01% respectively. Degradation kinetics studies found that electrolysis, adsorption, and biodegradation pathways play a major role in the degradation of cyclohexanone. Microbial community analysis indicates that voltage can affect the structure of the microbial community, with the dominant genera shifting from Acidovorax (0 V) to Brevundimonas (0.7 V). Additionally, Acidovorax, Cupriavidus, Ralstonia, and Hydrogenophaga have high abundance in the biofilm and can effectively metabolize cyclohexanone and its intermediates, facilitating the removal of cyclohexanone. In summary, this research can guide the development and construction of highly stable EBF systems and is expected to be used for advanced treatment of industrial wastewater containing cyclohexanone.
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  • 文章类型: Journal Article
    电化学氧化(EO),电子芬顿(EF),已对具有BDD阳极的光电Fenton(PEF)进行了比较评估,以从实际原水中修复RedCL和/或RedWB偶氮染料的溶液。对于pH3.0的50mMNa2SO4中的EO过程,主要氧化剂是阳极产生的异质•OH,而在EF和PEF中,H2O2的阴极产生和0.50mMFe2催化剂的添加还产生了均相·OH,从而增强了有机物的氧化。在PEF中,用6W的UVA光照射该溶液。用200mgL-1两种染料的1:1混合物在60分钟内总是发现几乎完全变色,其效率按EO Electrochemical oxidation (EO), electro-Fenton (EF), and photoelectro-Fenton (PEF) with a BDD anode have been comparatively assessed to remediate solutions of Red CL and/or Red WB azo dyes from real raw water. For the EO process in 50 mM Na2SO4 at pH 3.0, the main oxidant was the heterogeneous •OH generated at the anode, whereas in EF and PEF, the cathodic production of H2O2 and the addition of 0.50 mM Fe2+ catalyst additionally originated homogeneous •OH that enhanced the oxidation of organics. In PEF, the solution was illuminated with a 6 W UVA light. An almost total discoloration was always found operating with a 1:1 mixture of 200 mg L-1 of both dyes in 60 min, whose efficiency increased in the order of EO < EF < PEF. The HPLC analysis of the dye mixture treated by PEF disclosed that its degradation process agreed with its discoloration. A high 74% of COD was reduced due to the oxidative action of hydroxyl radicals and the photolysis of final Fe(III)-carboxylate species with UVA irradiation. The process was accompanied by an energy consumption of 0.76 kWh (g COD)-1, a value similar to the energy consumed by the applied UVA light.
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  • 文章类型: Journal Article
    必须为废水中的高电离电位(IP)有机污染物设计有效的去除策略,因为它们的电子供给能力降低了高级氧化系统的降解效率。在这种背景下,精心利用金属基碳材料结构,我们使用金属-吡啶-N(M-N-C,M=Fe,Co,和Ni)作为电子转移桥。这种独特的设计促进了电子从吸附剂表面到高IP值污染物表面的有序转移,作为“补充”来弥补它们不足的电子供给能力,从而最终导致这些污染物的选择性吸附。此外,该吸附剂还显示出有效去除痕量新出现的污染物(2mg/L),对各种盐表现出强大的抵抗力,表现出可重用性,并保持稳定。这些发现对未来的碳基材料设计具有重要意义。为处理水污染提供了一条通往卓越吸附性能的途径。
    It is imperative to devise effective removal strategies for high ionization potential (IP) organic pollutants in wastewater as their reduced electron-donating capacity challenges the efficiency of advanced oxidation systems in degradation. Against this backdrop, leveraging the metal-based carbon material structure meticulously, we employed metal-pyridine-N (M-N-C, M=Fe, Co, and Ni) as the electron transfer bridge. This distinctive design facilitated the ordered transfer of electrons from the adsorbent surface to the surface of high IP value pollutants, acting as a \"supplement\" to compensate for their deficient electron-donating capability, thereby culminating in the selective adsorption of these pollutants. Furthermore, this adsorbent also demonstrated effective removal of trace emerging contaminants (2 mg/L), displayed robust resistance to various salts, exhibited reusability, and maintained stability. These findings carry substantial implications for future carbon-based material design, offering a pathway toward exceptional adsorption performance in treating water pollution.
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  • 文章类型: Journal Article
    排放到下水道系统的工业废水通常具有高硝酸盐含量和低C/N比的特点。导致使用常规活性污泥法时处理成本高。本研究引入了部分反硝化-厌氧氨氧化(PD/A)颗粒工艺来应对这一挑战。PD/A颗粒工艺在2.3的低C/N比下实现了3.7mg/L的流出物TN水平。对典型循环的分析表明,部分反硝化在15分钟内达到峰值,硝酸盐与亚硝酸盐的转化率为86.9%。Anammox,从15到120分钟激活,贡献了86.2%的TN去除。该系统从有机休克后迅速恢复,这归因于TB-EPS中蛋白质含量的显着增加。颗粒共存后观察到微生物分散和重组,Thauera(39.12%)和CandidatusBrocadia(1.25%)被确定为关键的功能微生物。这项研究强调了PD/A颗粒污泥技术处理低C/N硝酸盐废水的有效性。
    Industrial wastewater discharged into sewer systems is often characterized by high nitrate contents and low C/N ratios, resulting in high treatment costs when using conventional activated sludge methods. This study introduces a partial denitrification-anammox (PD/A) granular process to address this challenge. The PD/A granular process achieved an effluent TN level of 3.7 mg/L at a low C/N ratio of 2.3. Analysis of a typical cycle showed that the partial denitrification peaked within 15 min and achieved a nitrate-to-nitrite transformation ratio of 86.9%. Anammox, which was activated from 15 to 120 min, contributed 86.2% of the TN removal. The system exhibited rapid recovery from post-organic shock, which was attributed to significant increases in protein content within TB-EPS. Microbial dispersion and reassembly were observed after coexistence of the granules, with Thauera (39.12%) and Candidatus Brocadia (1.25%) identified as key functional microorganisms. This study underscores the efficacy of PD/A granular sludge technology for treating low-C/N nitrate wastewater.
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  • 文章类型: Journal Article
    生物基絮凝剂在废物资源化利用和环境保护方面的研究已引起广泛关注。生物基絮凝剂包括植物基絮凝剂,以动物为基础,以及通过生物方法制备和修饰的微生物变体,化学,物理方法。这些絮凝剂具有丰富的官能团,独特的结构,和鲜明的特点。本文综合论述了生物基絮凝剂对常规污染物和新兴污染物的去除率,这些絮凝剂和污染物之间的相互作用,它们对废水处理中絮凝性能的影响,以及他们的应用成本。此外,它描述了生物基絮凝剂在实际应用中面临的共同挑战,以及解决这些挑战的各种改进策略。有了他们的安全档案,环境友好,效率,可再生性,以及来自不同来源的广泛可用性,生物基絮凝剂在废水处理中具有广泛使用的巨大潜力。
    The research on bio-based flocculants for waste resource utilization and environmental protection has garnered significant attention. Bio-based flocculants encompass plant-based, animal-based, and microbial variants that are prepared and modified through biological, chemical, and physical methods. These flocculants possess abundant functional groups, unique structures, and distinctive characteristics. This review comprehensively discussed the removal rates of conventional pollutants and emerging pollutants by bio-based flocculants, the interaction between these flocculants and pollutants, their impact on flocculation performance in wastewater treatment, as well as their application cost. Furthermore, it described the common challenges faced by bio-based flocculants in practical applications along with various improvement strategies to address them. With their safety profile, environmental friendliness, efficiency, renewability, and wide availability from diverse sources, bio-based flocculants hold great potential for widespread use in wastewater treatment.
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  • 文章类型: Journal Article
    藻-菌协同系统(ABSS)污水处理技术是一种具有低能耗,良好的处理效果和可回收的高价值产品。在这种治疗技术中,ABSS的建设是一个非常重要的因素。同时,一些新技术的出现(如微生物燃料电池和生物载体,等。)进一步丰富了小说ABSS的构建,提高了污水处理效率和生物质收获率。因此,本文着重介绍了新型ABSS在废水处理中的构建,以期为废水处理技术提供有用的建议。
    The wastewater treatment technology of algae-bacteria synergistic system (ABSS) is a promising technology which has the advantages of low energy consumption, good treatment effect and recyclable high-value products. In this treatment technology, the construction of an ABSS is a very important factor. At the same time, the emergence of some new technologies (such as microbial fuel cells and bio-carriers, etc.) has further enriched constructing the novel ABSS, which could improve the efficiency of wastewater treatment and the biomass harvesting rate. Thus, this review focuses on the construction of a novel ABSS in wastewater treatment in order to provide useful suggestions for the technology of wastewater treatment.
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  • 文章类型: Journal Article
    探索广阔的地外空间是人类不断发展的必然趋势。在可预见的未来将建立的宇宙飞船或长期使用的空间基地中,有限和封闭的空间中,水处理和再利用至关重要。自首次载人航天成功发射以来,专用水处理技术经历了60多年的迭代发展。在这里,我们简要回顾了相关的废水特性和空间站水处理的历史,我们专注于未来的挑战和前景,旨在为未来优化废水处理技术和关闭水循环提供见解。
    Exploring the vast extraterrestrial space is an inevitable trend with continuous human development. Water treatment and reuse are crucial in the limited and closed space that is available in spaceships or long-term use space bases that will be established in the foreseeable future. Dedicated water treatment technologies have experienced iterative development for more than 60 years since the first manned spaceflight was successfully launched. Herein, we briefly review the related wastewater characteristics and the history of water treatment in space stations, and we focus on future challenges and perspectives, aiming at providing insights for optimizing wastewater treatment technologies and closing the water cycle in future.
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  • 文章类型: Journal Article
    在废水处理中使用基于生物炭的催化剂已经付出了大量的努力。凭借其丰富的官能团和较高的比表面积,生物炭作为催化剂具有重要的前景。本文提出了一个全面的系统回顾和文献计量分析,涵盖了2009年至2024年期间,重点是通过生物炭催化恢复废水。生产,激活,彻底检查了用于生物炭的功能化技术。此外,先进技术的应用,如先进氧化工艺(AOPs),催化还原反应,并讨论了基于生物炭的生化驱动过程,重点阐明了生物炭的潜在机理以及表面官能团如何影响生物炭的催化性能。此外,利用生物炭的潜在缺点也被揭示出来。为了强调在这一研究领域取得的进展,并为未来的研究人员提供有价值的见解,使用CiteSpace和VOSviewer软件对595篇文章进行了科学计量分析。希望,这篇综述将加强对污染物处理中生物炭基催化剂的催化性能和机理的理解,同时为该领域未来的研究和开发工作提供视角和指导方针。
    A significant amount of effort has been devoted to the utilization of biochar-based catalysts in the treatment of wastewater. By virtue of its abundant functional groups and high specific surface area, biochar holds significant promise as a catalyst. This article presents a comprehensive systematic review and bibliometric analysis covering the period from 2009 to 2024, focusing on the restoration of wastewater through biochar catalysis. The production, activation, and functionalization techniques employed for biochar are thoroughly examined. In addition, the application of advanced technologies such as advanced oxidation processes (AOPs), catalytic reduction reactions, and biochemically driven processes based on biochar are discussed, with a focus on elucidating the underlying mechanisms and how surface functionalities influence the catalytic performance of biochar. Furthermore, the potential drawbacks of utilizing biochar are also brought to light. To emphasize the progress being made in this research field and provide valuable insights for future researchers, a scientometric analysis was conducted using CiteSpace and VOSviewer software on 595 articles. Hopefully, this review will enhance understanding of the catalytic performance and mechanisms pertaining to biochar-based catalysts in pollutant treatment while providing a perspective and guidelines for future research and development efforts in this area.
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