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Multifunctional solar evaporator: Directional freezing engineering for concurrent freshwater and electricity production with antibacterial property 多功能太阳能蒸发器:具有抗菌性能的淡水和电力同步生产的定向冷冻工程
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-14 DOI: 10.1016/j.jece.2026.121240
Zhen Li , Zhaoping Song , Jiebin Tang , Xi Gong , Huili Wang , Wenxia Liu
Limited evaporation rates, the threat of bacterial contamination, and the low utilization efficiency of electric potential generated during solar evaporation significantly hinder the development of evaporation processes—particularly in scenarios such as seawater treatment, industrial wastewater processing, and rural applications. In this work, a directionally frozen, architected solar-driven interfacial evaporator was prepared, which can achieve simultaneous high-efficiency evaporation, photocatalytic antibacterial function, and electric potential generation. Specifically, black titanium dioxide (B-TiO2) with excellent antibacterial properties was firstly prepared using a high-temperature reduction method. TEMPO (2,2,6,6-tetramethylpiperidin-1-oxyl)-oxidized cellulose nanofiber nanoparticles (TOCNFs) incorporated with Polyacrylamide (PAAm) to prepare PAAm/TOCNFs (PT) hydrogel evaporator. Subsequently, B-TiO2 was coated onto the surface of the PT hydrogel to improve its light-to-heat conversion capability, then finally obtained the B-TiO2@PAAm/TOCNFs (PTBT) solar evaporator. The introduction of TOCNFs increased the evaporation rate to 3.94 kg·m−2·h−1, and decreased the latent heat of water in the PTBT evaporator to 889.75 kJ·kg−1. Benefiting from the photocatalytic antibacterial properties of B-TiO2, the antibacterial efficiency of PTBT against E. coli and S. aureus reached 99.9 % and 99.8 %, respectively. Additionally, during the evaporation process, the PTBT evaporator exhibited salt tolerance and generated an open-circuit voltage as high as 184 mV. The combination of efficient solar evaporation with superior antibacterial properties is significant for improving solar energy utilization. This technology also holds significant potential for electricity generation via water evaporation.
有限的蒸发速率、细菌污染的威胁以及太阳能蒸发过程中产生的电势的低利用效率严重阻碍了蒸发过程的发展,特别是在海水处理、工业废水处理和农村应用等场景中。本工作制备了一种定向冷冻、构架式太阳能驱动界面蒸发器,该蒸发器可以同时实现高效蒸发、光催化抗菌和电势生成。其中,首次采用高温还原法制备了具有优异抗菌性能的黑色二氧化钛(B-TiO2)。TEMPO(2,2,6,6-四甲基胡椒碱-1-氧基)氧化纤维素纳米纤维纳米粒子(TOCNFs)与聚丙烯酰胺(PAAm)包合制备PAAm/TOCNFs (PT)水凝胶蒸化器。随后,将B-TiO2涂覆在PT水凝胶表面,提高其光热转换能力,最终得到B-TiO2@PAAm/TOCNFs (PTBT)太阳能蒸发器。TOCNFs的引入使蒸发速率提高到3.94 kg·m−2·h−1,使PTBT蒸发器中的水潜热降低到889.75 kJ·kg−1。利用B-TiO2的光催化抑菌特性,PTBT对大肠杆菌和金黄色葡萄球菌的抑菌效率分别达到99.9 %和99.8 %。此外,在蒸发过程中,PTBT蒸发器表现出耐盐性,并产生高达184 mV的开路电压。高效的太阳能蒸发与优越的抗菌性能相结合,对提高太阳能的利用率具有重要意义。这项技术还具有通过水蒸发发电的巨大潜力。
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引用次数: 0
Dynamics of engineered nanomaterials in the rhizosphere: Bidirectional feedback orchestrating multiscale responses 根际中工程纳米材料的动力学:双向反馈协调多尺度响应
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-12 DOI: 10.1016/j.jece.2026.121159
Weicheng Cao , Meng Qin , Yiting Wu , Qingyan Yu , Zhangchunzi Zhao , Xiaodong Nie , Zhongwu Li
Engineered nanomaterials (ENMs) hold transformative potential for diverse applications such as precision agriculture and soil remediation. However, assessing their subsequent ecological impacts, particularly within the dynamic rhizosphere, is complicated by complex feedback interactions among abiotic soil factors and plant-microbial dynamics. This review establishes a bidirectional feedback framework to elucidate how ENMs reshape rhizosphere microhabitats and, conversely, how soil-plant-microbe crosstalk dictates ENMs fates. Within this framework, soil properties, microbial extracellular matrices and root exudate chemodynamics emerge as master regulators of ENMs transformation cascades, thereby redefining paradigms of nanoecotoxicity and the associated feedback loops. Further, this review proposes the nano-feedback threshold (NFT) hypothesis, suggesting that microbial functional redundancy, plant tolerance and the chemodiversity of soil factors jointly buffer ENMs perturbations until a threshold is crossed, triggering cascading ecosystem reorganization. Critically, interdisciplinary integration approaches integrating multi-scale and multi-dimensional perspectives are necessary for decoding the feedback loops and NFT of ENMs in the rhizosphere. This review provides a conceptual basis for innovative ENMs development and identifies key strategies for leveraging ecologically balanced nanotechnology to support the achievement of Sustainable Development Goals in a changing climate.
工程纳米材料(enm)在精准农业和土壤修复等多种应用中具有变革潜力。然而,评估它们的后续生态影响,特别是在动态根际,是非生物土壤因子和植物-微生物动力学之间复杂的反馈相互作用是复杂的。这篇综述建立了一个双向反馈框架来阐明enm如何重塑根际微生境,反过来,土壤-植物-微生物串扰如何决定enm的命运。在此框架下,土壤特性、微生物胞外基质和根分泌物化学动力学成为enm转化级联的主要调节因子,从而重新定义纳米生态毒性的范式和相关的反馈回路。此外,本文提出了纳米反馈阈值(NFT)假说,认为微生物功能冗余、植物耐受性和土壤因子的化学多样性共同缓冲ENMs扰动,直到超过阈值,触发级联生态系统重组。重要的是,跨学科的整合方法整合了多尺度和多维视角,对于解码根际enm的反馈回路和NFT是必要的。这篇综述为创新的纳米技术发展提供了概念基础,并确定了利用生态平衡的纳米技术在不断变化的气候条件下支持实现可持续发展目标的关键战略。
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引用次数: 0
A review of cyanide-containing wastewater: Sources, hazard and treatment methods 含氰废水的来源、危害及处理方法综述
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-19 DOI: 10.1016/j.jece.2026.121344
Pengyi Wang , Acong Chen , Huihuan Lian , Shah Muhammad Ahmadzai , Fenglin Chang , Yi Pan , Yidi Chen , Bin Zhang , Huabin Zeng , Chaohai Wei
Cyanide is regarded as one of the key prebiotic compounds potentially involved in the origin of life on Earth, but it is also a hazardous pollutant with toxic effects on human health and the environment. Before discharge, cyanide-containing wastewater must be treated to mitigate its harmful impact. This article summarizes research achievements over the past five years alongside established disposal methods. Cyanide-containing wastewater is classified into two categories based on its source: exogenous addition and endogenous generation. Subsequently, the environmental hazards and biological toxicity of cyanide-containing wastewater are evaluated. The stability of cyanide compounds and the reasons behind the difficulties in treating this wastewater are also explored. Treatment methods are categorized according to their underlying principles as physical methods, chemical oxidation methods, chemical precipitation methods, and biological treatment methods. The treatment efficacy and costs associated with these different methods are systematically compared.
氰化物被认为是可能参与地球生命起源的关键益生元化合物之一,但它也是一种对人类健康和环境具有毒性影响的有害污染物。含氰废水在排放前必须经过处理,以减轻其有害影响。本文总结了近五年来的研究成果,并建立了处理方法。含氰废水按其来源可分为外源添加和内源生成两类。随后,对含氰废水的环境危害和生物毒性进行了评价。探讨了氰化物的稳定性及其处理困难的原因。处理方法根据其基本原理分为物理方法、化学氧化法、化学沉淀法和生物处理方法。系统比较了这些不同方法的治疗效果和费用。
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引用次数: 0
Potential and challenges of medium-chain fatty acids production from waste activated sludge using piezoelectric materials 利用压电材料从废活性污泥中生产中链脂肪酸的潜力和挑战
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-29 DOI: 10.1016/j.jece.2026.121480
Jiawei Liu , Xiangkun Li , Pengwei Xu , Ningxin Hu , Hao Ren , Gaige Liu
Efficient resource recovery of waste activated sludge (WAS) is essential for advancing circular economy and reducing environmental burdens. Traditional anaerobic fermentation suffers from low-value products and high separation costs, while medium-chain fatty acids (MCFAs) have attracted considerable attention as high-value chemicals. However, the dense extracellular polymeric substances (EPS) in sludge and the electron transfer bottleneck in anaerobic metabolism limit the synthesis efficiency of MCFAs. This study proposes a novel strategy for synergistically enhancing MCFAs production from sludge using piezoelectric materials: initially, at the physicochemical level, piezoelectric materials generate reactive oxygen species (ROS) through mechanical stress to break down the EPS barrier; subsequently, at the biological level, modified piezoelectric materials function as both “electronic bridges” and “field-effect generators” to enhance extracellular electron transfer (EET), promoting carbon flow towards the reverse β-oxidation (RBO) and fatty acid biosynthesis (FAB) pathways. Future research should focus on improving material stability and conducting technical-economic analysis to ensure the feasibility of this technology in practical sludge treatment.
有效回收废弃活性污泥是推进循环经济、减轻环境负担的重要手段。传统的厌氧发酵存在产品价值低、分离成本高的问题,而中链脂肪酸作为高价值化学品受到了广泛的关注。然而,污泥中密集的胞外聚合物(EPS)和厌氧代谢中的电子转移瓶颈限制了MCFAs的合成效率。本研究提出了一种利用压电材料协同提高污泥中MCFAs产量的新策略:首先,在物理化学水平上,压电材料通过机械应力产生活性氧(ROS)来打破EPS屏障;随后,在生物水平上,改性压电材料作为“电子桥”和“场效应发生器”,增强细胞外电子转移(EET),促进碳向反向β氧化(RBO)和脂肪酸生物合成(FAB)途径流动。未来的研究重点应放在提高材料稳定性和进行技术经济分析上,以确保该技术在实际污泥处理中的可行性。
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引用次数: 0
Synergistic effect of Bi₂MoO₆ and expanded MoS₂ heterostructures for highly efficient visible-light-driven environmental remediation Bi₂MoO₆与膨胀MoS₂异质结构的协同效应在高效可见光环境修复中的应用
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-13 DOI: 10.1016/j.jece.2025.120830
Magdeline Tze Leng Lai , Bao Lee Phoon , Kian Mun Lee , Chin Wei Lai , Mohd Rafie Johan , Supakorn Boonyuen , Joon Ching Juan
A series of Bi₂MoO₆/interlayer-expanded MoS₂ (BM-IEM) heterostructures was synthesized via a two-step hydrothermal method and evaluated for visible-light-driven methylene blue (MB) photodegradation. The 3 wt% BM–IEM composite achieved the highest photocatalytic efficiency, removing 98.2 % of MB in 60 min and sustaining its photocatalytic performance through five continuous cycles. This superior enhanced activity results from the strong interfacial coupling of Bi₂MoO₆ with the expanded MoS₂ structure, thereby enlarging the interlayer spacing, increasing the surface area, and creating strong electronic coupling at the Bi–O–S–Mo interface. These features enhance light absorption, facilitate charge separation, and promote the generation of reactive oxygen species (ROS). Oxygen-vacancy (OV) formation within the composite introduces mid-gap states that extend light responsiveness and support efficient electron transfer to adsorbed O₂, forming superoxide (•O₂⁻) and hydroxyl (•OH) radicals. The photocatalytic mechanism was analyzed through radical trapping and LC-MS experiments, revealing degradation pathways involving ring-opening oxidation, hydroxylation, and N-demethylation. The results demonstrate that tailoring interlayer spacing and defect states in MoS₂-based heterojunctions provides an effective design strategy for high-performance, visible-light-responsive photocatalysts for wastewater purification.
采用两步水热法合成了一系列Bi₂MoO₆/层间膨胀MoS₂(BM-IEM)异质结构,并对其可见光降解亚甲基蓝(MB)的性能进行了评价。3 wt%的BM-IEM复合材料具有最高的光催化效率,在60 min内去除98.2% %的MB,并在连续5个循环中保持其光催化性能。这种优异的增强活性是由于Bi₂MoO₆与膨胀后的MoS₂结构发生了强的界面耦合,从而扩大了层间距,增加了表面积,并在Bi - o - s - mo界面产生了强的电子耦合。这些特性增强了光吸收,促进了电荷分离,促进了活性氧(ROS)的产生。复合材料中的氧空位(OV)形成引入了中间间隙态,延长了光响应性,并支持有效的电子转移到吸附的O₂上,形成超氧(•O₂⁻)和羟基(•OH)自由基。通过自由基捕获和LC-MS实验分析了光催化机理,揭示了开环氧化、羟基化和n -去甲基化的降解途径。结果表明,调整MoS 2基异质结的层间间距和缺陷状态为设计高性能、可见光响应的废水净化光催化剂提供了有效的策略。
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引用次数: 0
Sludge-derived hydrochar enhances anaerobic digestion of sludge with tetracycline: Focusing on synergistic mechanism and microbial response 污泥衍生碳氢化合物增强污泥与四环素厌氧消化:聚焦协同机制和微生物响应
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-15 DOI: 10.1016/j.jece.2026.121256
Jiaojiao Shi , Guoqing Li , Saiyu Yuan , Zhouyang Lian , Shengwei Wang , Huiwen Zhang
Anaerobic digestion is an effective strategy for the degradation of organic matter and recovery of high value-added products. While the inhibitory effect of antibiotics such as tetracycline (TC) on anaerobic digestion is known, and though biochar-based carriers have been explored to mitigate such inhibition, the potential of hydrocha to simultaneously remove antibiotics and enhance microbial activity remains unclear. In this study, sludge-derived hydrothermal carbon prepared with rice husk (SHC-IV) was applied as a bio-carrier to enhance the anaerobic digestion performance of tetracycline(TC)-contaminated sludge. Results showed that moderate TC addition (TC100) improved methane production, with a maximum cumulative yield of 44.97 mL/g·VS, 15.89 % higher than the Raw. The incorporation of SHC-IV further enhanced hydrolysis, acidogenesis, and methanogenesis, with the TC50 +SHC-IV achieving the highest improvement (7.61 %) compared to TC50 alone. Microbial diversity analysis revealed that TC and SHC-IV increased Chao1 and Shannon indices, indicating enhanced microbial richness and diversity. TC addition shifted the dominant methanogen from Methanosaeta to Methanobacterium, while SHC-IV enriched Syntrophomonas and Methanosarcina, promoting syntrophic interactions and optimizing the methanogenic pathway. Furthermore, SHC-IV addition enhanced the removal of TC, with the TC50 +SHC-IV group reaching the highest removal increase of 4.93 % compared to TC50 alone. These findings demonstrate that SHC-IV not only mitigates the environmental risks of TC in sludge but also enhances anaerobic digestion performance, offering a sustainable approach for in-plant sludge hydrothermal product utilization.
厌氧消化是有机物降解和高附加值产品回收的有效策略。虽然抗生素如四环素(TC)对厌氧消化的抑制作用是已知的,尽管已经探索了基于生物炭的载体来减轻这种抑制,但水茶同时去除抗生素和增强微生物活性的潜力仍不清楚。本研究以稻壳制备的污泥源水热炭(SHC-IV)为生物载体,提高了四环素(TC)污染污泥的厌氧消化性能。结果表明,适度添加TC (TC100)提高了甲烷产量,最大累积产率为44.97 mL/g·VS,比Raw提高15.89 %。SHC-IV的掺入进一步增强了水解、产酸和产甲烷,与单独TC50相比,TC50 +SHC-IV获得了最高的改善(7.61 %)。微生物多样性分析显示,TC和SHC-IV增加了Chao1和Shannon指数,表明微生物丰富度和多样性增强。TC的加入使优势产甲烷菌从甲烷osaeta向甲烷杆菌转移,而SHC-IV则使Syntrophomonas和Methanosarcina富集,促进了共生相互作用,优化了产甲烷途径。此外,添加SHC-IV可以促进TC的去除,其中TC50 +SHC-IV组的去除率最高,比单独添加TC50的去除率提高4.93 %。这些研究结果表明,SHC-IV不仅可以减轻污泥中TC的环境风险,还可以提高厌氧消化性能,为厂内污泥热液产物的可持续利用提供了途径。
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引用次数: 0
The critical role of alkaline microenvironment in advanced oxidation processes: A case study of calcium carbonate polymorphs 碱性微环境在深度氧化过程中的关键作用:以碳酸钙多晶体为例
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-12 DOI: 10.1016/j.jece.2026.121182
Ziyang Chu , Haibo Liu , Tianhu Chen , Xuehua Zou , Fuwei Sun , Dong Chen
The microenvironment at the solid–liquid interface plays a pivotal role in activating peroxymonosulfate (PMS). This study quantitatively compared the alkaline microenvironments on calcite (Cal), aragonite (Ara), and vaterite (Vtr) surfaces, regarding their efficacy in activating PMS for Cu-EDTA decomplexation and Cu removal. Among these polymorphs, the Vtr/PMS system achieved the highest Cu-EDTA decomplexation (90.5 %) and Cu removal efficiency (84.6 %). Quenching tests, probe-based kinetic modeling and EPR experiments identified singlet oxygen (1O2) as the dominant reactive species across all systems, with the Vtr/PMS system generating the highest 1O2 exposure (1.21 ×10−8 M·s). Moreover, in-situ analysis of the interfacial microenvironment revealed that the Vtr/PMS system created a significantly more alkaline microenvironment (pH = 9.87), characterized by a rapid diffusion velocity of 34 μm/s. This pronounced alkaline microenvironment exhibited a strong positive correlation with the accelerated production of 1O2, thereby promoting Cu-EDTA decomplexation. Furthermore, the Cu removal mechanism in the Vtr/PMS system involved a synergistic process combining adsorption, coprecipitation, and structural incorporation of Cu2+ during the transformation of Vtr into calcite. This work highlights the critical role of the alkaline microenvironment in carbonate mineral-based catalysis.
固液界面微环境对过氧单硫酸盐(PMS)的活化起关键作用。本研究定量比较了方解石(Cal)、文石(Ara)和水晶石(Vtr)表面的碱性微环境对激活PMS进行Cu- edta解解和Cu去除的效果。在这些多态性中,Vtr/PMS体系具有最高的Cu- edta解解率(90.5 %)和Cu去除率(84.6 %)。淬火试验、基于探针的动力学建模和EPR实验表明,单线态氧(1O2)是所有体系中的主要反应物质,其中Vtr/PMS体系产生的1O2暴露量最高(1.21 ×10−8 M·s)。此外,现场微环境分析表明,Vtr/PMS系统创造了一个碱性更强的微环境(pH = 9.87),其扩散速度为34 μm/s。这种明显的碱性微环境与1O2的加速产生,从而促进Cu-EDTA的分解具有很强的正相关。此外,在Vtr/PMS体系中,Cu的去除机制涉及到Vtr转化为方解石过程中Cu2+的吸附、共沉淀和结构结合的协同过程。这项工作强调了碱性微环境在碳酸盐矿物基催化中的关键作用。
{"title":"The critical role of alkaline microenvironment in advanced oxidation processes: A case study of calcium carbonate polymorphs","authors":"Ziyang Chu ,&nbsp;Haibo Liu ,&nbsp;Tianhu Chen ,&nbsp;Xuehua Zou ,&nbsp;Fuwei Sun ,&nbsp;Dong Chen","doi":"10.1016/j.jece.2026.121182","DOIUrl":"10.1016/j.jece.2026.121182","url":null,"abstract":"<div><div>The microenvironment at the solid–liquid interface plays a pivotal role in activating peroxymonosulfate (PMS). This study quantitatively compared the alkaline microenvironments on calcite (Cal), aragonite (Ara), and vaterite (Vtr) surfaces, regarding their efficacy in activating PMS for Cu-EDTA decomplexation and Cu removal. Among these polymorphs, the Vtr/PMS system achieved the highest Cu-EDTA decomplexation (90.5 %) and Cu removal efficiency (84.6 %). Quenching tests, probe-based kinetic modeling and EPR experiments identified singlet oxygen (<sup>1</sup>O<sub>2</sub>) as the dominant reactive species across all systems, with the Vtr/PMS system generating the highest <sup>1</sup>O<sub>2</sub> exposure (1.21 ×10<sup>−8</sup> M·s). Moreover, <em>in-situ</em> analysis of the interfacial microenvironment revealed that the Vtr/PMS system created a significantly more alkaline microenvironment (pH = 9.87), characterized by a rapid diffusion velocity of 34 μm/s. This pronounced alkaline microenvironment exhibited a strong positive correlation with the accelerated production of <sup>1</sup>O<sub>2</sub>, thereby promoting Cu-EDTA decomplexation. Furthermore, the Cu removal mechanism in the Vtr/PMS system involved a synergistic process combining adsorption, coprecipitation, and structural incorporation of Cu<sup>2+</sup> during the transformation of Vtr into calcite. This work highlights the critical role of the alkaline microenvironment in carbonate mineral-based catalysis.</div></div>","PeriodicalId":15759,"journal":{"name":"Journal of Environmental Chemical Engineering","volume":"14 2","pages":"Article 121182"},"PeriodicalIF":7.2,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145981408","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Calcium transformation and product evolution behaviors in maleic acid–mediated indirect CO2 mineralization of carbide slag 马来酸介导的电石渣间接CO2矿化过程中钙的转化及产物演化行为
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-13 DOI: 10.1016/j.jece.2026.121204
Zhenwu Shi , Zhihui Shen , Jianlong Wang , Bingjie Zhou , Hanchi Wang
Indirect carbonation of carbide slag (CS) offers a promising route for simultaneous CO2 sequestration and value-added utilization of CS. Identifying a leaching agent that also enables controlled mineralization is the key to process performance. This study investigated Ca transformation and product evolution behaviors during maleic acid (MA)-mediated CS indirect carbonation. The results show that Ca extraction increases significantly with increasing MA concentration and leaching time, reaching a maximum of 97.89 % at a MA/Ca molar ratio of 2:1 for 5 min. Excess MA causes a decrease in Ca extraction due to supersaturation and precipitation of Ca(HC4H2O4)2. Ca2+ transition pathway during CO2 mineralization depends strongly on the initial solution pH. At pH 9–12, the high activity of HCO3 leads to Ca2+ precipitation into CaC4H2O4·2 H2O. Interestingly, as pH exceeds 13, persistent dominance of CO32 over solution speciation drives rapid amorphous CaCO3 nucleation and CaC4H2O4·2 H2O dissolution, ultimately forming calcite via dissolution–reprecipitation mechanism. Moreover, CaCO3 nucleation and growth balance control carbonation efficiency and product morphology. An 85.11 % of carbonation efficiency with nano-calcite can be obtained at 35°C for 35 min with a CO2 flow rate of 0.5 L/min. Furthermore, Ca2+ conversion and crystal aspect ratio both increase with increasing temperature, resulting in a carbonation efficiency over 90 % with abundant aragonite at 75°C. Efficient CO2 sequestration and nano-CaCO3 can be achieved simultaneously from CS with MA mediation and conditions regulation. This study reveals the MA-mediated indirect carbonation mechanism, providing solvent selection guidance and theoretical basis for efficient carbon fixation and value-added utilization of CS.
电石渣间接碳化为电石渣的同时固碳和增值利用提供了一条很有前途的途径。确定一种能够控制矿化的浸出剂是工艺性能的关键。研究了马来酸介导的CS间接碳酸化过程中Ca的转化和产物演化行为。结果表明:随着MA浓度的增加和浸出时间的延长,Ca的提取率显著提高,当MA/Ca摩尔比为2:1时,浸出时间为5 min, Ca的提取率达到97.89 %。过量的MA会导致Ca(HC4H2O4)2的过饱和和沉淀,从而降低Ca的萃取量。在CO2矿化过程中,Ca2+的过渡途径强烈依赖于初始溶液pH。在pH 9-12时,HCO3−的高活性导致Ca2+沉淀成CaC4H2O4·2 H2O。有趣的是,当pH超过13时,CO32−对溶液形态的持续优势驱动CaCO3快速非晶态成核和CaC4H2O4·2 H2O溶解,最终通过溶解-再沉淀机制形成方解石。CaCO3的成核和生长平衡控制着碳化效率和产物形态。在35℃、35 min、CO2流速0.5 L/min条件下,纳米方解石的碳化效率可达85.11 %。此外,Ca2+转化率和晶体长径比均随温度升高而增加,在75℃时碳化效率超过90 %,文石含量丰富。在MA的调解和条件调节下,CS可以同时实现高效的CO2固存和纳米caco3。本研究揭示了ma介导的间接碳化机理,为CS的高效固碳和增值利用提供了溶剂选择指导和理论依据。
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引用次数: 0
Efficient biodegradation and decolorization of azo dyes using peroxidase/chitosan-based enzyme-assisted coagulation 过氧化物酶/壳聚糖酶辅助混凝对偶氮染料的高效生物降解和脱色
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-14 DOI: 10.1016/j.jece.2026.121235
Na-won Baek , Shin-hee Lee
This study presents a novel enzyme-assisted coagulation (EAC) system as a low-carbon, energy-free strategy for the efficient treatment of azo dyes in textile wastewater. The EAC system integrates enzymatic oxidation with natural polymer-based coagulation and operates effectively under mild conditions without external energy input. Using horseradish peroxidase (HRP) and chitosan as model components, the system was applied to three representative azo dyes—Allura Red, Eriochrome Black, and Sunset Yellow—achieving decolorization efficiencies exceeding 98 %. Analytical techniques, including UV–Vis spectroscopy, FTIR, HPLC, and GC–MS, confirmed effective dye degradation and the stable aggregation of byproducts. The EAC mechanism involves the dual functionality of chitosan, which initially acts as an adsorbent and flocculant to enhance enzyme accessibility and subsequently serves as a stabilizing matrix that immobilizes and facilitates the removal of degradation products. This synergistic interaction between HRP and chitosan offers an efficient, biodegradable, and environmentally friendly approach for sustainable dye wastewater treatment.
本研究提出了一种新的酶辅助混凝(EAC)系统,作为一种低碳,无能源的策略,用于有效处理纺织废水中的偶氮染料。EAC系统将酶促氧化与天然聚合物混凝结合在一起,无需外部能量输入即可在温和条件下有效运行。以辣根过氧化物酶(HRP)和壳聚糖为模型组分,对三种具有代表性的偶氮染料——紫红、Eriochrome Black和Sunset yellow进行了脱色,脱色效率达到98% %以上。分析技术,包括紫外可见光谱、红外光谱、高效液相色谱和气相色谱-质谱,证实了染料的有效降解和副产物的稳定聚集。EAC机制涉及壳聚糖的双重功能,它最初作为吸附剂和絮凝剂,以提高酶的接近性,随后作为稳定基质,固定和促进降解产物的去除。HRP和壳聚糖之间的协同作用为染料废水的可持续处理提供了一种高效、可生物降解和环境友好的方法。
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引用次数: 0
Enhancement of MOF loading on fibrous membranes via construction of hierarchical porous structure for efficient uranium adsorption in aqueous solutions 通过构建分层多孔结构增强纤维膜上的MOF负载,以有效吸附水溶液中的铀
IF 7.2 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-04-01 Epub Date: 2026-01-14 DOI: 10.1016/j.jece.2026.121261
Yiting Lin , Yuhan Zhang , Zhaoxuan Duan , Yufei Zou , Shanshan Li , Zhenbo Cao
Efficient separation of uranium from aqueous solutions is of critical importance for environmental safety, yet it remains a significant scientific challenge. Adsorption by MOF-based fibrous membranes has attracted extensive interest for uranium separation due to its high efficiency and ease of scalability. However, the adsorption performance of these composite membranes greatly depends on the MOF loading. In this study, cellulose acetate electrospun membranes with a hierarchical porous structure (P-CA) were innovatively employed as substrates, enabling the preparation of composite membranes (P-CA@ZIF-67) with enhanced ZIF-67 loading (68.7 wt%). The synergistic effect of the abundant porosities and oxygen-containing groups in CA substrate membranes plays an important role in achieving high ZIF-67 loading. As expected, the P-CA@ZIF-67 membrane exhibits a prominent adsorption capacity for uranyl ions (684.9 mg/g at pH 3.0) and rapid kinetics (equilibrium time: 40 min). Furthermore, the uranium capacity retains 91 % of its initial value after five cycles, and an excellent uranium adsorption capacity of 1.22 mg/g is achieved after a 24-hour immersion in simulated seawater. These results highlight the application potential of the prepared membranes in the field of uranium adsorption from aqueous solutions. Meanwhile, the proposed strategy may present a new approach for fabricating efficient MOF-based fibrous membranes.
从水溶液中高效分离铀对环境安全至关重要,但它仍然是一个重大的科学挑战。mof基纤维膜吸附铀因其高效、易于扩展而受到广泛关注。然而,这些复合膜的吸附性能很大程度上取决于MOF的负载。在本研究中,创新地采用具有分层多孔结构(P-CA)的醋酸纤维素电纺丝膜作为底物,制备了具有增强ZIF-67负载(68.7 wt%)的复合膜(P-CA@ZIF-67)。CA底物膜中丰富的孔隙和含氧基团的协同作用是实现ZIF-67高负载的重要因素。正如预期的那样,P-CA@ZIF-67膜对铀酰离子具有显著的吸附能力(pH为3.0时为684.9 mg/g)和快速的吸附动力学(平衡时间为40 min)。在模拟海水中浸泡24小时后,铀的吸附容量达到1.22 mg/g,且经过5次循环后,铀的吸附容量保持在初始值的91 %。这些结果突出了所制备膜在水溶液中铀吸附领域的应用潜力。同时,该方法为制备高效mof基纤维膜提供了新的途径。
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Journal of Environmental Chemical Engineering
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