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Recent advances on magnetic carbon-related materials in advanced oxidation processes of emerging pollutants degradation 磁性碳相关材料在降解新兴污染物的高级氧化过程中的最新进展
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2024-01-09 DOI: 10.1016/j.wri.2024.100241
Elvana Çako , Kumaravel Dinesh Gunasekaran , Saravanan Rajendran , Anna Zielińska-Jurek

Recently, carbon-related materials have been proposed to improve the charge separation of the photogenerated carriers in the semiconductor matrices’ and surface properties. Carbon-related materials may act as co-catalysts, enhancing the pollutants adsorption on the surface, improving the charge carriers separation and photocatalyst stability and providing more active centres for photocatalytic reactions. This review summarizes recent advances in the preparation and environmental application of carbon-related materials. The focus was set on preparation of carbon-related materials and magnetic carbon-related photocatalytic materials with the property of easy separation after the purification process in an external magnetic field and their application for degradation of emerging pollutants not susceptible to biodegradation. The present studies identify four main groups of water pollutants: pesticides, pharmaceuticals, industrial chemicals, and heavy metals. Among them, pharmaceuticals and phenolic compounds represent a significant group of persistent organic pollutants. Some of the commonly used pharmaceuticals for human health, as well as disinfectants, are found in wastewater influents and effluents (after the purification process) almost in the unchanged form. Their detection in trace amounts (of about a few micrograms to hundreds of nanograms per litre) and removal become difficult but important because they put at risk the reuse of treated wastewater and the sustainability of water cycle management. Concerning levels of concentrations, these compounds are classified as hazardous due to possibilities of bioaccumulation, biomagnification and toxic impact on living organisms, even in trace amounts. Up to now, various methods have been reported in the removal of pharmaceuticals and phenolic compounds from aqueous systems.

Heterogeneous photocatalysis belonging to the group of advanced oxidation processes (AOPs) is one of the most promising methods used for the degradation of emerging pollutants. Introducing carbon-related materials modified by magnetic ferrites can significantly improve the efficiency of emerging contaminants' degradation. This review provides coherent information for future studies in the application of carbon-related materials and magnetic carbon-related materials for the removal of active pharmaceutical ingredients and phenolic compounds. Insights on pharmaceutical and phenolic compounds photodegradation in the presence of carbon-based materials combined with magnetic ferrites and their combination with SR-(AOPs) and Fenton-type photocatalysis are for the first time discussed. Moreover, the effect of various parameters such as water matrice, pH, natural organic matter presence, and temperature were also discussed. Finally, the economic feasibility and consideration of photocatalyst recovery capability completed the concept and discussion on magnetic carbon-related materials.

最近,有人提出利用碳相关材料来改善半导体基质中光生载流子的电荷分离和表面特性。碳相关材料可作为辅助催化剂,增强表面对污染物的吸附,改善电荷载流子的分离和光催化剂的稳定性,并为光催化反应提供更多的活性中心。本综述总结了碳相关材料的制备和环境应用方面的最新进展。重点是制备碳相关材料和磁性碳相关光催化材料,这些材料具有在外加磁场中净化后易于分离的特性,并可用于降解新出现的不易被生物降解的污染物。目前的研究确定了四大类水污染物:农药、药物、工业化学品和重金属。其中,药物和酚类化合物是一类重要的持久性有机污染物。一些对人类健康有益的常用药物和消毒剂几乎以未改变的形式存在于废水进水和出水(净化过程后)中。痕量(每升约几微克到几百毫微克)的检测和清除变得困难而重要,因为它们会危及废水处理后的再利用和水循环管理的可持续性。就浓度水平而言,这些化合物被归类为有害物质,因为即使是微量的,也有可能对生物体产生生物累积、生物放大和毒性影响。属于高级氧化过程(AOPs)的异相光催化是用于降解新兴污染物的最有前途的方法之一。引入经磁性铁氧体修饰的碳相关材料可以显著提高新兴污染物的降解效率。本综述为今后应用碳相关材料和磁性碳相关材料去除活性药物成分和酚类化合物的研究提供了连贯的信息。文章首次讨论了在碳基材料与磁性铁氧体结合以及它们与 SR-(AOPs) 和 Fenton 型光催化结合的情况下药物和酚类化合物的光降解问题。此外,还讨论了各种参数的影响,如水母质、pH 值、天然有机物的存在和温度。最后,经济可行性和光催化剂回收能力的考虑完成了磁性碳相关材料的概念和讨论。
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引用次数: 0
Electrochemical oxidation of losartan on a BDD electrode: Influence of cathodes and electrolytes on the degradation kinetics and pathways BDD 电极上的洛沙坦电化学氧化:阴极和电解质对降解动力学和途径的影响
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2024-01-05 DOI: 10.1016/j.wri.2024.100240
Rebecca Dhawle , Ardiana Kajtazi , Maria Sakellariou , Zacharias Frontistis , Frederic Lynen , Dionissios Mantzavinos

In this work, the influence of supporting electrolytes (sodium sulfate and sodium chloride) on the electrochemical oxidation of the antihypertensive drug losartan (LOS) was studied under different operating conditions such as current density (4.1–12.5 mA cm−2), electrolyte concentration (0.05–0.5 M), initial pollutant concentration (250–1000 μg L−1) and solution pH. The role of cathodes on the removal of LOS has been investigated using five different cathodes with carbonaceous cathodes showing better LOS removal. The effect of matrix composition has been studied using simulated water spiked with various constituents and real water matrices such as bottled water (BW) and wastewater (WW). The removal of LOS was pronounced while using a chloride electrolyte as compared to the sulfate electrolyte. The apparent rate constant increased on adding persulfate (PS) up to concentrations of 150 mg L−1 and decreased in the presence of bicarbonates and organic matter. The transformation products (TPs) formed during the electrochemical oxidation depended on the supporting electrolyte and two common TPs were identified in both electrolytes with a total of 4 TPs identified in the chloride medium and 7 TPs in the sulfate medium. Degradation pathways for LOS in both electrolytes have also been proposed.

在这项工作中,研究了在不同的操作条件下,如电流密度(4.1-12.5 mA cm-2)、电解质浓度(0.05-0.5 M)、初始污染物浓度(250-1000 μg L-1)和溶液 pH 值,支撑电解质(硫酸钠和氯化钠)对抗抑郁药物洛沙坦(LOS)电化学氧化的影响。使用五种不同的阴极研究了阴极对去除 LOS 的作用,其中碳质阴极对 LOS 的去除效果更好。使用添加了各种成分的模拟水以及瓶装水(BW)和废水(WW)等真实水基质研究了基质成分的影响。与硫酸盐电解质相比,氯化物电解质对 LOS 的去除效果更明显。加入浓度为 150 毫克/升-1 的过硫酸盐(PS)时,表观速率常数会增加,而加入碳酸氢盐和有机物时,表观速率常数会降低。电化学氧化过程中形成的转化产物(TPs)取决于支持电解质,在两种电解质中都发现了两种常见的 TPs,在氯化物介质中发现了 4 种 TPs,在硫酸盐介质中发现了 7 种 TPs。此外,还提出了 LOS 在两种电解质中的降解途径。
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引用次数: 0
Tailoring photocatalytic performance through Fe-doped TiO2/ZnO for effective remediation of organic contaminants 通过掺杂铁的 TiO2/ZnO 调整光催化性能,有效修复有机污染物
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2024-01-04 DOI: 10.1016/j.wri.2024.100239
Yalda Davoodi, Mohammad Saleh Shafeeyan

The development of highly efficient photocatalysts holds significant promise for addressing contemporary environmental challenges. This study focuses on the synthesis and characterization of a novel photocatalyst, iron-doped TiO2/ZnO particles, created through the sol-gel technique. The incorporation of iron ions into the crystalline structure of TiO2/ZnO aims to enhance the photocatalytic efficiency of TiO2. The findings revealed that Fe–ZnO/TiO2 exhibits a more thermally stable lattice compared to TiO2/ZnO, thereby retarding the phase transformation from anatase to rutile under higher calcination temperature. The photocatalytic performance of the synthesized photocatalyst was evaluated through the degradation of methyl orange under visible light irradiation. A statistical response surface methodology based on a central composite design was employed to develop a predictive model for color removal (as the dependent variable) considering variations in irradiation intensity, initial color concentration, catalyst concentration, reaction time, and pH (as independent variables). The analysis of variance identified the initial color concentration as the most influential factor, negatively affecting the predicted response. The experimental values of color removal exhibited good agreement with the predicted values from the regression model with a coefficient of determination of 0.949, indicating the accuracy of this model in predicting the mentioned outcomes. The presented model indicated that, for a sample of methyl orange with an initial concentration of 21.97 ppm, a reaction time of 117.69 min under direct irradiation of 21.63 W, a catalyst concentration of 0.61 g/L, and a pH of 4.74, the optimal color removal efficiency of 78.99 % was achieved.

高效光催化剂的开发为应对当代环境挑战带来了巨大希望。本研究的重点是通过溶胶-凝胶技术合成一种新型光催化剂--掺铁 TiO2/ZnO 粒子,并对其进行表征。在 TiO2/ZnO 的晶体结构中加入铁离子旨在提高 TiO2 的光催化效率。研究结果表明,与 TiO2/ZnO 相比,Fe-ZnO/TiO2 的晶格具有更高的热稳定性,因此在较高的煅烧温度下可延缓从锐钛型向金红石型的相变。通过在可见光照射下降解甲基橙,评估了合成光催化剂的光催化性能。考虑到辐照强度、初始颜色浓度、催化剂浓度、反应时间和 pH 值(作为自变量)的变化,采用了基于中心复合设计的统计响应面方法,建立了颜色去除(作为因变量)的预测模型。方差分析结果表明,初始颜色浓度是影响最大的因素,对预测反应有负面影响。除色的实验值与回归模型的预测值非常吻合,决定系数为 0.949,表明该模型在预测上述结果方面非常准确。该模型表明,对于初始浓度为 21.97 ppm 的甲基橙样品,在 21.63 W 的直接辐照下,反应时间为 117.69 分钟,催化剂浓度为 0.61 g/L,pH 值为 4.74,最佳除色效率为 78.99%。
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引用次数: 0
Modeling and optimization of efficient removal of diclofenac and naproxen based on chemometric approaches 基于化学计量学方法的双氯芬酸和萘普生高效去除模型的建立和优化
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2024-01-01 DOI: 10.1016/j.wri.2023.100238
Seyyed Amirreza Abdollahi , Amirasad Pourabadeh , Mahsa Alishiri , Abolfazl Sodagartojgi , Seyyed Faramarz Ranjbar , Mir Biuok Ehghaghi , Faramarz Talati

This work investigated the efficiency of CoFe2O4 nanoparticles in removing diclofenac and naproxen drugs from aqueous solutions. At first, the Taguchi method was performed to choose the most important factors among the investigated factors affecting the removal efficacy of these drugs. Afterward, the optimal conditions of the effective factors were investigated and modeled by the central composite design-based response surface method. The results revealed that the maximum drug removal was obtained at pH = 7, temperature of 25 °C, adsorbent dosage of 215 mg, sonication time of 21 min, and diclofenac and naproxen concentrations of 15 mg L−1. The removal efficacy of diclofenac and naproxen under these optimal conditions was 99.42 % and 95.11 %, respectively. Based on the results, it is concluded that CoFe2O4 nanoparticles can be applied as an easy-available and effective adsorbent for removing diclofenac and naproxen from water samples.

本研究探讨了 CoFe2O4 纳米粒子去除水溶液中双氯芬酸和萘普生药物的效率。首先,采用田口方法从影响这些药物去除效果的考察因素中选择最重要的因素。然后,采用基于中心复合设计的响应面法对有效因素的最佳条件进行了研究和建模。结果表明,在 pH = 7、温度为 25 °C、吸附剂用量为 215 毫克、超声时间为 21 分钟、双氯芬酸和萘普生浓度为 15 毫克/升时,药物去除率最大。在这些最佳条件下,双氯芬酸和萘普生的去除率分别为 99.42 % 和 95.11 %。根据这些结果,可以得出结论:CoFe2O4 纳米粒子可作为一种易得且有效的吸附剂,用于去除水样中的双氯芬酸和萘普生。
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引用次数: 0
Investigating the biomass-specific inhibitory effect of benzalkonium chloride on anaerobic granules: A kinetic approach 研究苯扎氯铵对厌氧颗粒的生物质特异性抑制作用:动力学方法
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2023-12-12 DOI: 10.1016/j.wri.2023.100237
Sinem Fundneider-Kale , Vanessa Acevedo Alonso , Markus Engelhart

Benzalkonium Chloride (BAC), a quaternary ammonium compound commonly used in industrial disinfection processes, was studied for its biomass-specific inhibitory effect on the specific methanogenic activity (SMA) of anaerobic granules. Inhibition batch assays were conducted with varying BAC concentrations (5–40 mg/L), resulting in biomass-dependent inhibition. Considering its surface-active nature, a biomass-specific BAC load was a suitable parameter to determine IC50 values, ranging from 4.3 to 6.1 mg BAC/g VS. For predicting the corresponding biomass-specific inhibition constant in ADM1, the inclusion of an additional adsorption-inhibition term was required for a better validation of results. The model yielded a biomass-specific IC50 of 5.3 mg BAC/g VS. The results encourage a change in perspective on IC50 for surfactants by determining a biomass-specific IC50, particularly in scenarios when surfactants accumulate within anaerobic reactors. Hereby, the reliability and practical relevance of IC50 is increased, driving the development of mitigation strategies.

研究了工业消毒过程中常用的季铵类化合物苯扎氯铵(BAC)对厌氧颗粒特定产甲烷活性(SMA)的生物特异性抑制作用。在不同BAC浓度(5-40 mg/L)下进行了抑制批次试验,结果显示抑制依赖于生物量。考虑到其表面活性,生物量特异性BAC负荷是确定IC50值的合适参数,范围为4.3至6.1 mg BAC/g VS.为了预测ADM1中相应的生物量特异性抑制常数,需要包含额外的吸附抑制项以更好地验证结果。该模型得出了5.3 mg BAC/g vs的生物质特异性IC50,通过确定生物质特异性IC50,特别是在厌氧反应器中表面活性剂积累的情况下,结果鼓励了对表面活性剂IC50的看法的改变。因此,IC50的可靠性和实际相关性得到了提高,从而推动了缓解战略的发展。
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引用次数: 0
Examination of interactions between heavy metals and benzotriazoles in rainwater runoff and snowmelt in an urban catchment in Poland 波兰城市集水区雨水径流和融雪中重金属与苯并三唑之间相互作用的研究
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2023-12-07 DOI: 10.1016/j.wri.2023.100236
Maciej Bełcik , Martyna Grzegorzek , Fausto A. Canales , Joanna Struk-Sokołowska , Bartosz Kaźmierczak

Heavy metals (HMs) are toxic pollutants that can accumulate and harm human health and the environment. Monitoring their concentration in water is an essential tool for evaluating the quality and safety of this vital resource. The aims of this study were (i) to characterize HMs contamination in rainwater runoff and snowmelt, identify likely sources and compliance with regulations and guidelines, and (ii) to conduct a preliminary assessment regarding the potential link between the occurrence of HMs and benzotriazoles based on a previous experiment. This study investigates the concentration of six HMs (cadmium, lead, nickel, chromium, copper, and zinc) in rainwater runoff and snowmelt samples collected in twelve Białystok locations in northeastern Poland. The highest concentration of Cu (517.5 μg/L) was identified in snowmelt from the city's ring road, with heavy vehicle traffic, and near an industrial area. A 4-lane asphalt street near the city center exhibited the highest concentrations of Pb (91.1 μg/L) and Ni (64.6 μg/L) for snowmelt and also for Cd (1.37 μg/L) and Ni (27.3 μg/L) in rainwater runoff. A snowmelt sample from a pedestrian-only area in the city center presented the highest Zn concentration (3672.2 μg/L). Considerable contents of Cr (353.2 μg/L) were found in snowmelt near an industrial and warehousing area. Snowmelt presented higher HMs concentrations than rainwater runoff. Our results indicate that most benzotriazoles and heavy metals occur independently. The analysis of the winds and the tendency of HMs to travel with dust particles suggest that specific contaminants might have originated in Belarus, a neighboring territory of Białystok.

重金属 (HM) 是一种有毒污染物,可累积并危害人类健康和环境。监测水中的重金属浓度是评估这一重要资源的质量和安全性的重要工具。本研究的目的是:(i) 描述雨水径流和融雪中 HMs 污染的特征,确定可能的来源以及是否符合法规和指导原则;(ii) 根据之前的实验,对 HMs 的出现与苯并三唑之间的潜在联系进行初步评估。本研究调查了在波兰东北部比亚韦斯托克 12 个地点收集的雨水径流和融雪样本中六种 HMs(镉、铅、镍、铬、铜和锌)的浓度。在车辆通行繁忙的城市环路和工业区附近的融雪中发现了最高浓度的铜(517.5 μg/L)。市中心附近的一条四车道沥青街道的融雪中铅 (91.1 μg/L) 和镍 (64.6 μg/L) 的浓度最高,雨水径流中镉 (1.37 μg/L) 和镍 (27.3 μg/L) 的浓度也最高。市中心行人专用区的融雪水样本中的锌浓度最高(3672.2 微克/升)。在工业和仓储区附近的融雪中发现了相当高的铬含量(353.2 μg/L)。融雪的 HMs 浓度高于雨水径流。我们的研究结果表明,大多数苯并三唑和重金属是独立存在的。对风的分析以及 HMs 随灰尘颗粒移动的趋势表明,特定污染物可能来自比亚韦斯托克的邻近地区白俄罗斯。
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引用次数: 0
Electrochemical treatment of antibiotic wastewater containing ceftriaxone sodium by porous Ti/Magnéli Ti4O7 nanotube arrays 利用多孔钛/马涅利 Ti4O7 纳米管阵列对含有头孢曲松钠的抗生素废水进行电化学处理
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2023-12-02 DOI: 10.1016/j.wri.2023.100235
Yonghao Zhang, Yating Song, Liu Liu, Jie Zhang, Zhaoyi Zhang, Qian Li, Jing Yang, Wen Li, Lulu Huang, Xue Li, Yulei Zhang, Qiangshun Wu, Xuejie Guo

In this study, porous Ti/Magnéli Ti4O7 nanotube arrays (NTA) was fabricated to pretreat antibiotic wastewater. Characterization of the Ti4O7-NTA illustrated that highly ordered NTA was successfully generated on the porous Ti substrate, which enlarged the specific surface area by 1.67 times. The Ti4O7-NTA has a high oxygen evolution potential (2.60 V) as well as low interfacial charge transfer resistance (4.479 Ω cm−2). Ceftriaxone sodium (CRO) was completely removed from raw antibiotic wastewater after 3 h of treatment by the Ti4O7-NTA, under optimal operation conditions. The biodegradability and toxicity of the wastewater were also significantly enhanced and reduced, as the BOD/COD and EC50,48h values were increased to 0.48 and 57.62 % ± 2.16 %, respectively. The possible degradation pathway of CRO was proposed by LC‒MS. Cathodic polarization was proven to be an effective way to ensure the long-term durability of the Ti4O7-NTA.

本研究制作了多孔钛/马涅利 Ti4O7 纳米管阵列(NTA),用于抗生素废水的预处理。对 Ti4O7-NTA 的表征表明,在多孔 Ti 基质上成功生成了高度有序的 NTA,比表面积扩大了 1.67 倍。Ti4O7-NTA 具有较高的氧进化电位(2.60 V)和较低的界面电荷转移电阻(4.479 Ω cm-2)。在最佳操作条件下,Ti4O7-NTA 处理头孢曲松钠(CRO)3 小时后,可完全去除抗生素原废水中的头孢曲松钠。废水的生物降解性和毒性也显著提高和降低,BOD/COD 和 EC50,48h 值分别提高到 0.48 % 和 57.62 % ± 2.16 %。LC-MS 提出了 CRO 的可能降解途径。阴极极化被证明是确保 Ti4O7-NTA 长期耐久性的有效方法。
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引用次数: 0
Enhancing sonocatalytic dye pollutant degradation using MoS2/RGO nanocomposites: An optimization study 二硫化钼/还原氧化石墨烯纳米复合材料增强声催化降解染料污染物的优化研究
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2023-12-01 DOI: 10.1016/j.wri.2023.100223
Farid Ahani , Maisam Jalaly , Javad Moghaddam , Mohammad Hossein Rasoulifard

This research focuses on the synthesis of MoS2/RGO nanocomposite, which serves as an efficient sonocatalyst, using a simple one-step hydrothermal method. The MoS2/RGO was characterized through various techniques including X-ray diffraction (XRD), field-emission scanning electron microscope (FE-SEM), transmission electron microscope (TEM), Raman spectrometry, diffuse reflectance spectroscopy (DRS), and Fourier transform infrared (FTIR) spectroscopy. A comprehensive investigation into the sonocatalytic degradation efficiency of methylene blue (MB) dye was conducted under different conditions using design of experiment (DOE) approach. Response surface methodology (RSM) based on central composite design (CCD) was employed to optimize the key operational parameters, namely initial dye concentration, catalyst dosage, ultrasonic power, sonication time, and pH. The reliability of the model was assessed using analysis of variance. Under the optimal conditions of 20 mg/L initial MB concentration, catalyst dosage of 0.5 g/L, 67 W ultrasonic power, sonication time of 28 min, and pH of 7, a remarkable MB degradation efficiency of 99% was achieved. Hydroxyl radical (OH) were identified as the main radical species in the sonoluminescence reaction. Additionally, the sonocatalyst demonstrated an excellent reusability, with approximately 95% retention of the degradation efficiency observed over five sonocatalysis cycles.

本研究采用简单的一步水热法合成了MoS2/RGO纳米复合材料作为高效的声催化剂。通过x射线衍射(XRD)、场发射扫描电子显微镜(FE-SEM)、透射电子显微镜(TEM)、拉曼光谱、漫反射光谱(DRS)和傅里叶变换红外光谱(FTIR)等多种技术对MoS2/RGO进行了表征。采用实验设计法(DOE)对不同条件下亚甲基蓝(MB)染料的声催化降解效率进行了全面研究。采用基于中心复合设计(CCD)的响应面法(RSM)对初始染料浓度、催化剂用量、超声功率、超声时间和ph等关键操作参数进行优化,并通过方差分析对模型的可靠性进行评估。在初始MB浓度为20 mg/L、催化剂用量为0.5 g/L、超声功率为67 W、超声时间为28 min、pH为7的条件下,对MB的降解效率达到了99%。在声致发光反应中,羟基自由基(OH)是主要的自由基种类。此外,该声催化剂具有良好的可重复使用性,在5次声催化循环中,降解效率保持在95%左右。
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引用次数: 1
Stability of geothermal waters parameters as a major factor guaranteeing the possibility of its use and discharge into the environment 地热水参数的稳定性是保证地热水利用和向环境排放可能性的主要因素
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2023-11-23 DOI: 10.1016/j.wri.2023.100233
Agnieszka Operacz , Agnieszka Zachora-Buławska , Zuzanna Gonek , Barbara Tomaszewska , Bogusław Bielec , Tomasz Operacz , Jochen Bundschuh

Geothermal waters are considered a type of renewable energy source. Waters with elevated temperatures are also used in balneotherapy. In each type of use, the stability of the basic parameters guarantees the reliable operation of the plant. On the other hand, useable geothermal waters, which in legal terms are usually wastewater, are discharged into a surface water reservoir or injected into the rock. The diversity of geothermal waters use options creates the need to assess stability. Low and known variability of the basic parameters is extremely important for the protection of the receiving environment or the reliability of the injection process. This paper identifies the basic parameters, the relationships between them and a methodology for assessing their stability, which has not been widely used to date. The approach presented is universal and can be successfully applied to other geothermal installations anywhere in the world.

地热水被认为是一种可再生能源。水温升高的水也用于浴疗。在各种类型的使用中,基本参数的稳定是装置可靠运行的保证。另一方面,可用的地热水,在法律上通常是废水,被排放到地表水水库或注入岩石中。地热水使用方案的多样性产生了对其稳定性进行评估的必要性。基本参数的低和已知的可变性对于保护接收环境或注射过程的可靠性非常重要。本文确定了基本参数,它们之间的关系和一种评估其稳定性的方法,这种方法迄今尚未广泛使用。所提出的方法是通用的,可以成功地应用于世界上任何地方的其他地热设施。
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引用次数: 0
MXene-based composites for capacitive deionization – The advantages, progress, and their role in desalination - A review mxene基电容去离子复合材料的优点、进展及其在海水淡化中的应用综述
IF 5.1 3区 工程技术 Q1 WATER RESOURCES Pub Date : 2023-11-02 DOI: 10.1016/j.wri.2023.100230
Bakhtiar Ali Samejo , Kainat Naseer , Suraya Samejo , Farooque Ahmed Janjhi , Najma Memon , Roberto Castro-Muñoz , Grzegorz Boczkaj

MXenes, a novel large family of 2D transition metal carbides, carbonitrides and nitrides are currently a “hot topic” in science due to their several fascinating physical and chemical properties. It follows from a rich diversity of their elemental compositions and chemical functionalities. MXenes can form composites with many substances, including polymers or metal oxides, which allows to effective “tune” MXene characteristics to a fit-to-the-purpose applications. Capacitive deionization (CDI) is currently widely studied as advanced desalination technique due to the advantages of cost-effectiveness, eco-friendly, and high salt removal capacity. One of key fields for CDI development relates to the ion's intercalation materials as concept taken from the sodium ion batteries, which is used in CDI because of their excellent desalination capacity. These materials provide effective sodium ions removal from the brine based on intercalation mechanism as well as redox reactions. In this review, we timely review an up-to-date accomplishment in the advancement of distinct MXene-based composite materials used as CDI electrodes, along with discussion of fundamental electrochemical energy storage mechanisms. The most relevant outcomes are highlighted together with the phenomena observed when applied in desalination applications. Finally, potential solutions as well as challenges in this field are summarized.

MXenes是一种新的2D过渡金属碳化物,碳氮化物和氮化物家族,由于其几种迷人的物理和化学性质,目前是科学界的“热门话题”。这源于它们元素组成和化学功能的丰富多样性。MXene可以与多种物质形成复合材料,包括聚合物或金属氧化物,这使得MXene的特性可以有效地“调整”到适合用途的应用中。电容式去离子(CDI)作为一种先进的海水淡化技术,具有成本效益高、环境友好、除盐能力强等优点,目前得到了广泛的研究。离子嵌入材料是CDI发展的关键领域之一,其概念来源于钠离子电池,由于其优异的脱盐能力而被用于CDI。这些材料基于插层机理和氧化还原反应,能有效地去除盐水中的钠离子。在这篇综述中,我们及时回顾了用于CDI电极的不同mxene基复合材料的最新进展,并讨论了基本的电化学储能机制。重点介绍了最相关的结果以及在海水淡化应用中观察到的现象。最后,总结了该领域可能的解决方案和挑战。
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