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Nanoscale engineer: The revolutionary role of nanobubbles in the synthesis of functional nanomaterials 纳米工程师:纳米气泡在功能纳米材料合成中的革命性作用
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-04 DOI: 10.1016/j.desal.2024.118271
Yang Wu , Jiayin Zhang , Weixing Xu , Bin Li , Wei Zhang , Zhentao Wang , Haojie Xu , Junfeng Wang , Jianming Pan , Kai Yu
The study of bulk nanobubbles (NBs) has long been an interest of the scientific community. Recent studies have highlighted the revolutionary role of NBs as nanoscale engineers in the synthesis of functional nanomaterials in a sustainable, controllable and soft-template manner. In this process, the preparation and stability control of NBs is particularly critical, which directly determines the performance of the soft template and the quality and functionality of the final material. This review focuses on the key breakthroughs of NBs as green and soft templates for the fabrication of functional nanomaterials. The emerging technique, which allows for the control over the size, morphology, and properties of the nanomaterials by adjusting the characteristics of the bulk NBs templates, shows significant promise. The burgeoning preparation techniques for NBs, including physical and chemical methods, are first outlined. The application scenarios and relative merits of different NBs producing methods are compared and analyzed. Recent advances in the control of NBs stability are then discussed, considering the influence of temperature, pH, surfactant, electrolyte, and gas properties on NBs stability. Finally, the recent achievements of NBs-templated nanomaterials for the applications in uranium extraction, catalysis and desalination are emphasized, while the underlying mechanisms for material preparation and optimization are also discussed.
对体态纳米气泡(NBs)的研究一直是科学界的兴趣所在。最近的研究强调了 NBs 作为纳米级工程师在以可持续、可控制和软模板方式合成功能纳米材料中的革命性作用。在这一过程中,NB 的制备和稳定性控制尤为关键,它直接决定了软模板的性能以及最终材料的质量和功能。本综述重点介绍 NB 作为绿色软模板用于制造功能纳米材料的关键突破。这种新兴技术通过调整块状 NBs 模板的特性来控制纳米材料的尺寸、形态和性质,显示出巨大的前景。首先概述了新兴的 NBs 制备技术,包括物理和化学方法。比较并分析了不同 NBs 制备方法的应用场景和相对优势。然后,考虑到温度、pH 值、表面活性剂、电解质和气体特性对 NBs 稳定性的影响,讨论了在控制 NBs 稳定性方面的最新进展。最后,重点介绍了最近在铀萃取、催化和海水淡化领域应用 NBs 模板纳米材料的成果,并讨论了材料制备和优化的基本机制。
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引用次数: 0
AIE-derived fluorescent silsesquioxane-based hybrid aerogel for light-enhanced gold recovery 基于硅倍半氧烷的 AIE 衍生荧光混合气凝胶用于光增强黄金回收
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-04 DOI: 10.1016/j.desal.2024.118265
Mengshuang Zhang, Hongzhi Liu
In this work, two aggregation-induced emission (AIE)-active organic fluorescent monomers (TPV, TPC) were synthesized by Knoevenagel reaction of 2,2′-([1,1′-biphenyl]-4,4′-diyl)diacetonitrile with benzaldehyde and 4-bromobenzaldehyde, respectively. Subsequently, two fluorescent hybrid porous polymers with semiconductor performance (PCS-TPV, PCS-TPC) were prepared successfully by connecting octavinyl silsesquioxane (OVS) with TPV and TPC through Friedel-Crafts reaction and Heck coupling, respectively. Among them, PCS-TPV with a hyper-crosslinked structure offered a specific surface area of up to 1165 m2 g−1; PCS-TPC was the first AIE-derived fluorescent hybrid silsesquioxane-based semiconductor polymer with 3-D conjugated structure. Compared with PCS-TPV, PCS-TPC exhibited stronger visible light absorption, higher fluorescent performance and quantum yield due to its high AIE-active unit content. Besides, PCS-TPC exhibited a remarkable gold recovery capacity (Qm = 2728 mg g−1) when exposed to visible light irradiation. Adsorption mechanism revealed that the photoelectrons produced by PCS-TPC under visible light irradiation reduced all adsorbed Au(III) to Au(I) and Au(0). Furthermore, a hybrid aerogel was prepared through physical blending of PCS-TPC with chitosan, overcoming the limitation that insoluble powder was difficult to process and recycle. This work provided a very efficient, sustainable, and industrially feasible way for gold recovery in e-waste.
本研究通过 2,2′-([1,1′-联苯]-4,4′-二基)二乙腈分别与苯甲醛和 4-溴苯甲醛的克诺文纳格尔反应合成了两种具有聚集诱导发射(AIE)活性的有机荧光单体(TPV、TPC)。随后,辛钒基硅倍半氧烷(OVS)分别与 TPV 和 TPC 通过弗里德尔-卡夫斯反应和赫克偶联成功制备了两种具有半导体性能的荧光杂化多孔聚合物(PCS-TPV 和 PCS-TPC)。其中,PCS-TPV具有超交联结构,比表面积高达1165 m2 g-1;PCS-TPC是第一种由AIE衍生的具有三维共轭结构的硅倍半氧烷基荧光杂化半导体聚合物。与 PCS-TPV 相比,PCS-TPC 的 AIE 活性单元含量高,因此具有更强的可见光吸收能力、更高的荧光性能和量子产率。此外,当暴露在可见光照射下时,PCS-TPC 还表现出显著的金回收能力(Qm = 2728 mg g-1)。吸附机理显示,PCS-TPC 在可见光照射下产生的光电子将所有吸附的金(III)还原为金(I)和金(0)。此外,通过将 PCS-TPC 与壳聚糖进行物理混合,制备出了一种混合气凝胶,克服了不溶性粉末难以加工和回收的局限。这项工作为从电子垃圾中回收金提供了一种非常高效、可持续且在工业上可行的方法。
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引用次数: 0
Green and sustainable pH-responsive adsorptive membrane using aminated-MXene mangrove filled polylactic acid ultrafiltration membrane for enhanced water permeability and microplastic removal 利用胺化-MXene 红树林填充聚乳酸超滤膜提高透水性和微塑料去除率的绿色可持续 pH 响应吸附膜
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-03 DOI: 10.1016/j.desal.2024.118268
Fatema Khamis, Hanaa M. Hegab, Shadi W. Hasan
A green and sustainable pH-responsive adsorptive membrane using aminated-MXene mangrove filled (MXAM) polylactic acid ultrafiltration membrane was developed. The material synthesis involved employing the common in-situ HF acid-based etching method with Li+ intercalant, while membrane fabrication utilized the non-solvent induced phase inversion (NIPS) technique. The study tested pH-responsive adsorption and filtration using a 20 ppm synthetic polystyrene (PS) microplastic (MPs) suspension at pH 4, 7, and 10. Incorporating 1.5 wt% MXAM enhanced water permeability to 1855.6 LMHbar and achieved rejection rates of 79 %, 91.5 %, and 99.9 % for pH 4, 7, and 10, respectively. These improvements can be attributed to enhanced porosity, pore size, hydrophilicity, and surface charges. The kinetics of the adsorptive 1.5PLAMXAM membrane for PS MPs at 5 ppm and pH 7 showed psuedo-second-order kinetics (R2 = 0.967) matching experimental adsorption (qe,exp = 12.4 mg.g−1), indicating chemical adsorption. The equilibrium data of 1.5PLAMXAM membrane fitting the Langmuir isotherm, showed an increase in qe,exp from 5.69 to 12.79 mg.g−1 at pH 4 and 10, respectively, attributed to a higher density of pH-responsive groups. The fitted Langmuir isotherm suggested a maximum monolayer coverage of qm = 23.5 mg.g−1.
利用氨基化-MXene 红树林填充(MXAM)聚乳酸超滤膜开发了一种绿色、可持续的 pH 响应吸附膜。材料合成采用了常见的原位高频酸基蚀刻法,并添加了 Li+ 插层剂,而膜制造则采用了非溶剂诱导相反转(NIPS)技术。研究使用 20 ppm 合成聚苯乙烯(PS)微塑料(MPs)悬浮液在 pH 值为 4、7 和 10 的条件下测试了 pH 值响应吸附和过滤。加入 1.5 wt% 的 MXAM 可将透水性提高到 1855.6 LMHbar,pH 值为 4、7 和 10 时的排斥率分别为 79%、91.5% 和 99.9%。这些改进可归因于孔隙率、孔径、亲水性和表面电荷的增强。在 5 ppm 和 pH 值为 7 时,1.5PLAMXAM 膜对 PS MPs 的吸附动力学(R2 = 0.967)与实验吸附(qe,exp = 12.4 mg.g-1)相吻合,显示出化学吸附作用。拟合 Langmuir 等温线的 1.5PLAMXAM 膜的平衡数据显示,在 pH 值为 4 和 10 时,qe,exp 分别从 5.69 增加到 12.79 mg.g-1,这归因于 pH 反应基团的密度较高。拟合的朗缪尔等温线表明最大单层覆盖率为 qm = 23.5 mg.g-1。
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引用次数: 0
Supercapacitive behavior of two-dimensional carbon nanosheets with oxygen-induced interfacial modification 氧诱导界面修饰的二维碳纳米片的超级电容行为
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-02 DOI: 10.1016/j.desal.2024.118261
Zonglun Cao , Hailong Li , Yiyang Zhang , Yue Lian , Huaihao Zhang
Biomass-derived carbon typically contains abundant heteroatomic defects and interfacial functional groups, which can contribute to additional pseudocapacitance. However, the type of interfacial functional groups in biomass-derived carbon is uncontrollable and variable, reducing their homogeneity. In this work, recyclable boric acid was employed as an activator to convert bioaerogels into carbon nanosheets. Subsequently, low-temperature air oxidation was utilized to modulate their thickness and microstructure. Notably, the multiple and uncontrollable functional groups at the carbon interface were uniformly transformed into oxygen-containing functional groups under oxygen induction, resulting in 2D carbon nanosheet materials with enhanced stability properties. Meanwhile, the introduction of more oxygen-containing functional groups, such as carbonyl (C=O) and carboxyl (-COOH) groups, improves material wettability and capacitive properties. In addition, the boron and nitrogen elements doping introduced by activators and precursors enhances its pseudocapacitive properties and electrical conductivity from the carbon lattice perspective. Moreover, the rich electron/deficient effect of BN valence bond can effectively boost their conductivity and rate performance. In fact, the materials present good capacitive properties (high specific capacitance of 298.5 F g−1 in KOH three-electrode system) and CDI (capacitive deionization) performance (good desalting capacity of 35.2 mg g−1 in CDI system).
生物质衍生碳通常含有丰富的异原子缺陷和界面官能团,可产生额外的假电容。然而,生物质衍生碳中界面官能团的类型是不可控和可变的,这降低了它们的均匀性。在这项工作中,采用了可回收的硼酸作为活化剂,将生物气凝胶转化为碳纳米片。随后,利用低温空气氧化来调节其厚度和微观结构。值得注意的是,在氧气诱导下,碳界面上的多种不可控官能团被均匀地转化为含氧官能团,从而得到稳定性能更强的二维碳纳米片材料。同时,引入更多的含氧官能团,如羰基(C=O)和羧基(-COOH),可改善材料的润湿性和电容特性。此外,活化剂和前驱体引入的硼和氮元素掺杂也从碳晶格的角度增强了材料的伪电容特性和导电性。此外,BN 价键的富电子/缺电子效应可有效提高其导电性和速率性能。事实上,这些材料具有良好的电容特性(在 KOH 三电极系统中具有 298.5 F g-1 的高比电容)和 CDI(电容式去离子)性能(在 CDI 系统中具有 35.2 mg g-1 的良好脱盐能力)。
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引用次数: 0
Ladder electrodialysis: Efficient up-concentration of lithium ion and its mechanisms behind 阶梯电渗析:锂离子的高效浓缩及其背后的机制
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-02 DOI: 10.1016/j.desal.2024.118270
Cong Liu , Siyang Gu , Wenjing Gao , Ming Tan , Yong Lin , Min Hu , Yuebiao Li , Yang Zhang
The development of lithium extraction technology from salt lakes has seen significant demand in recent years, driven by the surge in energy storage needs for lithium-ion batteries used in electric vehicles and renewable power plants. Currently, evaporation technologies such as Mechanical Vapor Recompression (MVR) and Multi-Effect Distillation (MED) are commonly employed to concentrate lithium chloride for subsequent lithium carbonate precipitation. However, these evaporation methods limit lithium yield and increase capital and operational costs, particularly in high latitude areas. Pressure-driven membrane processes like reverse osmosis are hindered by concentration polarization and cannot significantly increase lithium chloride concentration. This study proposes a new membrane stack configuration with a laddered compartment design, termed Ladder Electrodialysis (LED), which addresses the concentration polarization issue and achieves a lithium salt (LiCl) concentration of 16.39 % (196 g·L−1). Economic analysis shows that the energy consumption is only 0.42 kWh per kilogram of LiCl. Ladder electrodialysis is a novel salt concentration technology, with applications in brine valorization or disposal.
近年来,由于电动汽车和可再生能源发电厂使用的锂离子电池储能需求激增,对盐湖提锂技术的开发需求巨大。目前,通常采用机械蒸汽再压缩(MVR)和多效蒸馏(MED)等蒸发技术来浓缩氯化锂,以便随后沉淀碳酸锂。然而,这些蒸发方法限制了锂的产量,增加了资本和运营成本,尤其是在高纬度地区。反渗透等压力驱动的膜过程受到浓缩极化的阻碍,无法显著提高氯化锂的浓度。本研究提出了一种新的膜堆配置,采用阶梯式隔室设计,称为阶梯电渗析(LED),可解决浓度极化问题,使锂盐(氯化锂)浓度达到 16.39 %(196 g-L-1)。经济分析表明,每公斤锂盐的能耗仅为 0.42 千瓦时。阶梯电渗析是一种新颖的盐浓缩技术,可应用于盐水提纯或处理。
{"title":"Ladder electrodialysis: Efficient up-concentration of lithium ion and its mechanisms behind","authors":"Cong Liu ,&nbsp;Siyang Gu ,&nbsp;Wenjing Gao ,&nbsp;Ming Tan ,&nbsp;Yong Lin ,&nbsp;Min Hu ,&nbsp;Yuebiao Li ,&nbsp;Yang Zhang","doi":"10.1016/j.desal.2024.118270","DOIUrl":"10.1016/j.desal.2024.118270","url":null,"abstract":"<div><div>The development of lithium extraction technology from salt lakes has seen significant demand in recent years, driven by the surge in energy storage needs for lithium-ion batteries used in electric vehicles and renewable power plants. Currently, evaporation technologies such as Mechanical Vapor Recompression (MVR) and Multi-Effect Distillation (MED) are commonly employed to concentrate lithium chloride for subsequent lithium carbonate precipitation. However, these evaporation methods limit lithium yield and increase capital and operational costs, particularly in high latitude areas. Pressure-driven membrane processes like reverse osmosis are hindered by concentration polarization and cannot significantly increase lithium chloride concentration. This study proposes a new membrane stack configuration with a laddered compartment design, termed Ladder Electrodialysis (LED), which addresses the concentration polarization issue and achieves a lithium salt (LiCl) concentration of 16.39 % (196 g·L<sup>−1</sup>). Economic analysis shows that the energy consumption is only 0.42 kWh per kilogram of LiCl. Ladder electrodialysis is a novel salt concentration technology, with applications in brine valorization or disposal.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"594 ","pages":"Article 118270"},"PeriodicalIF":8.3,"publicationDate":"2024-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142658850","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tailoring high-performance polyesteramide NF membranes for purifying natural surface water: Enhanced minerals preservation, chlorine resistance, and mechanisms 定制用于净化天然地表水的高性能聚酯酰胺无负压膜:强化矿物质保存、耐氯性和机制
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-02 DOI: 10.1016/j.desal.2024.118267
Xuewu Zhu , Feiyue Ge , Xinwei Kang , Liping Qiu , Bin Liu , Jingtao Xu , Feihong Wang , Daoji Wu , Zhe Yang , Daliang Xu , Heng Liang
Nanofiltration membranes (NF) possessing high flux, excellent selectivity, and chlorine resistance are urgently required for healthy drinking water treatment. In this work, we prepared a high-performance polyesteramide (PEA) nanofiltration membrane featuring polyester and polyamide composite structures using piperazine (PIP) and polyvinyl alcohol (PVA) as co-monomers via sodium hydroxide catalyzing interfacial polymerization. The resultant NF membranes' surface morphology, chemical structure, filtration performance, and chlorine stability were systematically evaluated. The optimized PEA membrane (PEA-TFC) possessed a terraced morphology and relatively high roughness (23.9 nm). During purifying real surface water, a high flux (20.29 LMH bar−1) with <50 % mineral rejection and over 70 % organic matter removal was achieved for PEA-TFC, demonstrating excellent organic/mineral selectivity. In addition, the polyamide and polyester structures provided uniform pore size distribution and fewer chlorine-active sites, granting PEA-TFC excellent chlorine resistance and stability. The exceptional organic/mineral selective separations and remarkable chlorine resistance endow the PEA-TFC as a promising candidate for healthy drinking water NF.
健康饮用水处理迫切需要具有高通量、优异选择性和耐氯性的纳滤膜(NF)。在这项工作中,我们以哌嗪(PIP)和聚乙烯醇(PVA)为共聚单体,通过氢氧化钠催化界面聚合,制备出了一种高性能聚酯酰胺(PEA)纳滤膜,它具有聚酯和聚酰胺复合结构。结果对 NF 膜的表面形态、化学结构、过滤性能和氯稳定性进行了系统评估。优化后的 PEA 膜(PEA-TFC)具有阶梯状形态和相对较高的粗糙度(23.9 nm)。在净化实际地表水的过程中,PEA-TFC 的通量很高(20.29 LMH bar-1),矿物质去除率为 50%,有机物去除率超过 70%,显示出卓越的有机物/矿物质选择性。此外,聚酰胺和聚酯结构提供了均匀的孔径分布和较少的氯活性位点,使 PEA-TFC 具有出色的耐氯性和稳定性。出色的有机物/矿物质选择性分离和显著的耐氯性使 PEA-TFC 成为健康饮用水 NF 的理想候选材料。
{"title":"Tailoring high-performance polyesteramide NF membranes for purifying natural surface water: Enhanced minerals preservation, chlorine resistance, and mechanisms","authors":"Xuewu Zhu ,&nbsp;Feiyue Ge ,&nbsp;Xinwei Kang ,&nbsp;Liping Qiu ,&nbsp;Bin Liu ,&nbsp;Jingtao Xu ,&nbsp;Feihong Wang ,&nbsp;Daoji Wu ,&nbsp;Zhe Yang ,&nbsp;Daliang Xu ,&nbsp;Heng Liang","doi":"10.1016/j.desal.2024.118267","DOIUrl":"10.1016/j.desal.2024.118267","url":null,"abstract":"<div><div>Nanofiltration membranes (NF) possessing high flux, excellent selectivity, and chlorine resistance are urgently required for healthy drinking water treatment. In this work, we prepared a high-performance polyesteramide (PEA) nanofiltration membrane featuring polyester and polyamide composite structures using piperazine (PIP) and polyvinyl alcohol (PVA) as <em>co</em>-monomers via sodium hydroxide catalyzing interfacial polymerization. The resultant NF membranes' surface morphology, chemical structure, filtration performance, and chlorine stability were systematically evaluated. The optimized PEA membrane (PEA-TFC) possessed a terraced morphology and relatively high roughness (23.9 nm). During purifying real surface water, a high flux (20.29 LMH bar<sup>−1</sup>) with &lt;50 % mineral rejection and over 70 % organic matter removal was achieved for PEA-TFC, demonstrating excellent organic/mineral selectivity. In addition, the polyamide and polyester structures provided uniform pore size distribution and fewer chlorine-active sites, granting PEA-TFC excellent chlorine resistance and stability. The exceptional organic/mineral selective separations and remarkable chlorine resistance endow the PEA-TFC as a promising candidate for healthy drinking water NF.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"593 ","pages":"Article 118267"},"PeriodicalIF":8.3,"publicationDate":"2024-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142578503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced electricity generation and energy storage in a microbial fuel cell with a bimetallic-modified capacitive anode 采用双金属改性电容阳极的微生物燃料电池可增强发电和储能能力
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-01 DOI: 10.1016/j.desal.2024.118247
Yuyang Wang , Su Ma , Lida Hou , Jinlong Zuo , Xiangquan Kong , Yu Song , Zhijie Wang , Ye Tian , Jing Dong
Microbial fuel cells (MFCs) are energy conversion devices that utilize microorganisms attached to the electrode as catalysts for the oxidation of organic waste, thereby generating electricity. In this study, a two-step hydrothermal method was employed to prepare a CF/NiO/Fe3O4 capacitive composite anode by directly growing NiO on a carbon felt substrate as a metal framework to support the in-situ growth of Fe3O4. In this paper, electrochemical tests such as cyclic voltammetry and AC impedance were used to investigate the electrochemical performance of the modified anode. The two electrodes were characterized by SEM, EDS, XRD, FTIR, BET, TEM and SAED test. The MFCs with the CF/NiO/Fe3O4 anode exhibited significant improvements in generation of power and storage of energy performance, reaching a maximum power density of 9.29 W/m3, which has increased by 1.54-fold compared to CF/NiO anode. After charging/discharging for 60 min, the CF/NiO/Fe3O4 anode had a sum charge of 8532.07C /m2, which was a significant increase of 1868.82C/m2 compared to the CF/NiO anode. High-throughput sequencing analysis suggested that the proportion of electricity-generating microorganisms on the CF/NiO/Fe3O4 surface of the anode reached 86.03 %, which was higher than that on CF/NiO anode surface. The protein contents of the CF/NiO/Fe3O4 reached 71.03 mg/cm3. The application of capacitive materials in MFCs would allow the constructed MFCs to generate and store bioelectricity simultaneously.
微生物燃料电池(MFC)是一种能量转换装置,利用附着在电极上的微生物作为催化剂氧化有机废物,从而产生电能。本研究采用两步水热法制备了 CF/NiO/Fe3O4 电容式复合阳极,方法是在碳毡基底上直接生长 NiO 作为金属框架,以支持 Fe3O4 的原位生长。本文采用循环伏安法和交流阻抗等电化学测试方法来研究改性阳极的电化学性能。通过扫描电镜、EDS、XRD、傅立叶变换红外光谱、BET、TEM 和 SAED 测试对两种电极进行了表征。采用 CF/NiO/Fe3O4 阳极的 MFC 在发电和储能性能方面都有显著改善,最大功率密度达到 9.29 W/m3,比 CF/NiO 阳极提高了 1.54 倍。充放电 60 分钟后,CF/NiO/Fe3O4 阳极的电荷总和为 8532.07C /m2,比 CF/NiO 阳极显著增加了 1868.82C/m2。高通量测序分析表明,CF/NiO/Fe3O4 阳极表面的发电微生物比例达到 86.03%,高于 CF/NiO 阳极表面。CF/NiO/Fe3O4 的蛋白质含量达到 71.03 mg/cm3。在 MFC 中应用电容材料可使构建的 MFC 同时产生和储存生物电。
{"title":"Enhanced electricity generation and energy storage in a microbial fuel cell with a bimetallic-modified capacitive anode","authors":"Yuyang Wang ,&nbsp;Su Ma ,&nbsp;Lida Hou ,&nbsp;Jinlong Zuo ,&nbsp;Xiangquan Kong ,&nbsp;Yu Song ,&nbsp;Zhijie Wang ,&nbsp;Ye Tian ,&nbsp;Jing Dong","doi":"10.1016/j.desal.2024.118247","DOIUrl":"10.1016/j.desal.2024.118247","url":null,"abstract":"<div><div>Microbial fuel cells (MFCs) are energy conversion devices that utilize microorganisms attached to the electrode as catalysts for the oxidation of organic waste, thereby generating electricity. In this study, a two-step hydrothermal method was employed to prepare a CF/NiO/Fe<sub>3</sub>O<sub>4</sub> capacitive composite anode by directly growing NiO on a carbon felt substrate as a metal framework to support the in-situ growth of Fe<sub>3</sub>O<sub>4</sub>. In this paper, electrochemical tests such as cyclic voltammetry and AC impedance were used to investigate the electrochemical performance of the modified anode. The two electrodes were characterized by SEM, EDS, XRD, FTIR, BET, TEM and SAED test. The MFCs with the CF/NiO/Fe<sub>3</sub>O<sub>4</sub> anode exhibited significant improvements in generation of power and storage of energy performance, reaching a maximum power density of 9.29 W/m<sup>3</sup>, which has increased by 1.54-fold compared to CF/NiO anode. After charging/discharging for 60 min, the CF/NiO/Fe<sub>3</sub>O<sub>4</sub> anode had a sum charge of 8532.07C /m<sup>2</sup>, which was a significant increase of 1868.82C/m<sup>2</sup> compared to the CF/NiO anode. High-throughput sequencing analysis suggested that the proportion of electricity-generating microorganisms on the CF/NiO/Fe<sub>3</sub>O<sub>4</sub> surface of the anode reached 86.03 %, which was higher than that on CF/NiO anode surface. The protein contents of the CF/NiO/Fe<sub>3</sub>O<sub>4</sub> reached 71.03 mg/cm<sup>3</sup>. The application of capacitive materials in MFCs would allow the constructed MFCs to generate and store bioelectricity simultaneously.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"593 ","pages":"Article 118247"},"PeriodicalIF":8.3,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142573033","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Capacitive deionization exploiting La-based LDH composite electrode toward energy efficient and selective removal of phosphate 利用 La 基 LDH 复合电极的电容式去离子技术,实现高效节能和选择性去除磷酸盐
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-01 DOI: 10.1016/j.desal.2024.118259
Chunming Feng , Xiaobing Pan , Xiaocheng Lin , Yi Yang , Fuqiang Fan , Chenxiao Jiang , Ying Mei
Capacitive deionization (CDI) is a promising technology for removing phosphate from wastewater. Its practical implementation is however hindered by the constraints on the electrode materials. To boost the adsorption capacity, phosphate selectivity, and cost-effectiveness of the electrode, this study proposed a composite electrode blending Lanthanum-based layered double hydroxide (Ca-La LDH) and activated carbon (AC). It capitalizes on the synergistic effects of electric double layer capacitance (EDLC) of AC and the diffusion-controlled charge storage (pseudocapacitive behavior) of Ca-La LDH. By optimizing the mass ratios of the constituents and the electrode material loading capacities, the composite electrode AC/Ca-La LDH-5020 was developed, which contains 20 mg of 50 wt% Ca-La LDH. This composition achieved a remarkable phosphate adsorption capacity of 34.8 mg P /g and a low energy consumption of 0.0051 kWh/g P in constant voltage (CV) mode. It represented a 241 % increase in adsorption capacity (mg P/g) and 71 % decrease in specific energy consumption (kWh/g P) compared to the electrode made solely of AC. Particularly the moderate inclusion of Lanthanum contributes to its cost-effectiveness. Moreover, further studies extensively examined the impacts of electrical driving force, including applied voltage in constant voltage (CV) mode and applied current in constant current (CC) mode, on the phosphate removal efficiency. The composite electrode remained stable performance with the presence of the high content of coexisting anions (e.g.,Cl,SO42−, HCO3, NO3), obtaining high selectivity coefficient of phosphate over other anions. This study highlighted the practical potential of AC/Ca-La LDH composite electrode for advancing CDI technology for phosphate removal in an efficient, energy-saving and cost-effective manner.
电容式去离子技术(CDI)是一种很有前途的去除废水中磷酸盐的技术。然而,电极材料的限制阻碍了该技术的实际应用。为了提高电极的吸附能力、磷酸盐选择性和成本效益,本研究提出了一种混合镧系双层氢氧化物(Ca-La LDH)和活性炭(AC)的复合电极。它充分利用了 AC 的双电层电容(EDLC)和 Ca-La LDH 的扩散控制电荷存储(伪电容行为)的协同效应。通过优化各成分的质量比和电极材料的负载能力,开发出了 AC/Ca-La LDH-5020 复合电极,其中含有 20 毫克 50 wt% 的 Ca-La LDH。在恒压(CV)模式下,这种成分的磷酸盐吸附容量高达 34.8 毫克 P/g,能耗低至 0.0051 千瓦时/克 P。与完全由交流电制成的电极相比,吸附容量(毫克磷/克)提高了 241%,比能耗(千瓦时/克磷)降低了 71%。镧的适度加入尤其有助于提高其成本效益。此外,进一步的研究还广泛考察了电驱动力(包括恒压(CV)模式下的施加电压和恒流(CC)模式下的施加电流)对磷酸盐去除效率的影响。在共存阴离子(如 Cl-、SO42-、HCO3-、NO3-)含量较高的情况下,复合电极仍能保持稳定的性能,对磷酸盐的选择性系数高于其他阴离子。这项研究凸显了 AC/Ca-La LDH 复合电极在推动 CDI 技术以高效、节能和经济的方式去除磷酸盐方面的实用潜力。
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引用次数: 0
Structure-function relationship for functional films with constructed graded channels in dye/salt separation and fouling resistance 在染料/盐分离和防污方面具有构造分级通道的功能薄膜的结构-功能关系
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-01 DOI: 10.1016/j.desal.2024.118262
Tianmeng Zhang , Weiwei Zhang , Xiaoyan Yang , Han Zuilhof , Hao Lu
The structural assembly of polypyrrole particle stacking, combined with polydopamine space-filling, forms composite film with a network of interconnected fluid channels. The composite films achieve high water flus, separation efficiency and ratio of organic dyes/inorganic salts (flux: >600 L m−2 h−1 bar−1; dye rejection: ~100 %; salt rejection: <5 %). Simulation using different dye fouling models show that the dye only interacts at the surface, and hardly affects internal pores of the film throughout the filtration process. Owing to the patterned surface structure as constructed by microsphere arrangement and inter-structure adaptation assembly, the functional film has excellent contamination tolerance and rinsing regeneration for macromolecular pollutants. The results of computational fluid dynamics simulations further indicate that the high shear stress above the microspheres with vortex flow in the interstitial space has a positive effect on reducing contaminant deposition. In addition to the separation property, the composite film shows good structural stability and mechanical strength in various complex water environments, benefiting their future practical applications. This work unveils the structure-function relationship for composite function films with constructed graded channels in dye/salt separation, which is important for the design and future application of these functional films.
聚吡咯粒子堆叠结构与聚多巴胺空间填充相结合,形成了具有相互连接的流体通道网络的复合薄膜。这种复合薄膜具有较高的水通量、分离效率和有机染料/无机盐比率(通量:>600 L m-2 h-1 bar-1;染料去除率:~100%;盐去除率:<5%):~100 %;盐分去除率:<5 %)。使用不同的染料堵塞模型进行的模拟显示,在整个过滤过程中,染料只在表面发生作用,几乎不影响薄膜的内部孔隙。由于微球排列和结构间适应性组装构建了图案化的表面结构,该功能膜对大分子污染物具有出色的耐污染性和漂洗再生能力。计算流体动力学模拟结果进一步表明,微球上方的高剪切应力和间隙空间的涡流对减少污染物沉积有积极作用。除了分离性能外,复合膜在各种复杂的水环境中还表现出良好的结构稳定性和机械强度,有利于其未来的实际应用。这项研究揭示了具有构造分级通道的复合功能薄膜在染料/盐分离中的结构-功能关系,这对这些功能薄膜的设计和未来应用具有重要意义。
{"title":"Structure-function relationship for functional films with constructed graded channels in dye/salt separation and fouling resistance","authors":"Tianmeng Zhang ,&nbsp;Weiwei Zhang ,&nbsp;Xiaoyan Yang ,&nbsp;Han Zuilhof ,&nbsp;Hao Lu","doi":"10.1016/j.desal.2024.118262","DOIUrl":"10.1016/j.desal.2024.118262","url":null,"abstract":"<div><div>The structural assembly of polypyrrole particle stacking, combined with polydopamine space-filling, forms composite film with a network of interconnected fluid channels. The composite films achieve high water flus, separation efficiency and ratio of organic dyes/inorganic salts (flux: &gt;600 L m<sup>−2</sup> h<sup>−1</sup> bar<sup>−1</sup>; dye rejection: ~100 %; salt rejection: &lt;5 %). Simulation using different dye fouling models show that the dye only interacts at the surface, and hardly affects internal pores of the film throughout the filtration process. Owing to the patterned surface structure as constructed by microsphere arrangement and inter-structure adaptation assembly, the functional film has excellent contamination tolerance and rinsing regeneration for macromolecular pollutants. The results of computational fluid dynamics simulations further indicate that the high shear stress above the microspheres with vortex flow in the interstitial space has a positive effect on reducing contaminant deposition. In addition to the separation property, the composite film shows good structural stability and mechanical strength in various complex water environments, benefiting their future practical applications. This work unveils the structure-function relationship for composite function films with constructed graded channels in dye/salt separation, which is important for the design and future application of these functional films.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"593 ","pages":"Article 118262"},"PeriodicalIF":8.3,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142572877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Computer modeling of employing binary/ternary organic blends in integrated HP-assisted HDH desalination systems 在集成式 HP 辅助 HDH 海水淡化系统中使用二元/三元有机混合物的计算机建模
IF 8.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-11-01 DOI: 10.1016/j.desal.2024.118260
Yanli Xu , Hui Li , Azher M. Abed , M.A. El-Shorbagy , Ashit Kumar Dutta , Sherzod Abdullaev , Hakim AL Garalleh , Rania Mona Alqaralleh , Yasser Elmasry , Albara Ibrahim Alrawashdeh
The global demand for potable water is rising, prompting the development of various energy systems for distilled water production. However, the significance of utilizing multicomponent working fluids in these systems has been largely overlooked. This study presents computer modeling of three HDH-based distillation units powered by two conventional heat pump cycles, namely, the simple and vapor injection heat pumps (first and second models) and an innovative heat pump cycle with an ejector expander (third model). The significance of the research lies in its pioneering investigation of utilizing two- and three-component mixtures in heat pump-based desalination units, which has not been previously explored. The study's primary aim is to determine whether using multicomponent working fluids instead of pure fluids or introducing structural modifications can more effectively enhance the performance of heat pump-based distillation units. The proposed models are simulated using EES and MATLAB software, with the study focusing on energetic, exergetic, exergoeconomic, and heat exchanger modeling to evaluate the feasibility of the configurations. The findings revealed that the structural modifications in the third scenario using R134a resulted in the highest GOR, with improvements of 44 % and 26.03 %, respectively, compared to the other scenarios. However, utilizing binary blend R22/R142b with different compositions improved the GOR of the first to three scenarios by 41.26 %, 29.06 %, and 11.87 %, respectively. Furthermore, in this case, the unit cost of distilled water for the first, second, and third scenarios increased by 12.87 %, 14.32 %, and 12.70 %, respectively. Finally, the first scenario has the highest NPV of 4.40 M$ and the shortest PP of 8.13 years. Therefore, utilizing the blend in a simple heat pump proves to be more efficient and cost-effective than implementing structural modifications.
全球对饮用水的需求不断增长,促使人们开发出各种用于蒸馏水生产的能源系统。然而,在这些系统中利用多组分工作流体的重要性在很大程度上被忽视了。本研究介绍了以两种传统热泵循环(即简单热泵和蒸汽喷射热泵(第一和第二种模式)以及带有喷射膨胀机的创新热泵循环(第三种模式))为动力的三种基于 HDH 的蒸馏装置的计算机建模。这项研究的意义在于,它开创性地研究了在基于热泵的海水淡化装置中利用双组分和三组分混合物的问题,而这在以前是没有过的。研究的主要目的是确定使用多组分工作流体代替纯流体或引入结构调整是否能更有效地提高基于热泵的蒸馏装置的性能。使用 EES 和 MATLAB 软件对所提出的模型进行了模拟,研究侧重于能量、能效、能效经济和热交换器建模,以评估配置的可行性。研究结果表明,在第三种方案中,使用 R134a 进行结构改造的 GOR 最高,与其他方案相比,分别提高了 44% 和 26.03%。然而,使用不同成分的 R22/R142b 二元混合物则使第一至三种方案的 GOR 分别提高了 41.26 %、29.06 % 和 11.87 %。此外,在这种情况下,第一、第二和第三种方案的蒸馏水单位成本分别增加了 12.87 %、14.32 % 和 12.70 %。最后,第一种方案的净现值最高,为 440 万美元,PP 期最短,为 8.13 年。因此,在简单的热泵中使用混合物比进行结构改造更有效、更经济。
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