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Effect of inoculum sources on caproic acid production from food waste through lactate-based chain elongation: Properties and microbial succession 接种物来源对通过乳酸盐链延伸从厨余垃圾中生产己酸的影响:特性和微生物演替
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114186

Caproic acid (CA) production is a promising way to valorize food waste (FW), but the low CA yield seriously restricts its application. Inoculum source as a key factor can affect the microbial communities and CA fermentation processes, but was not fully explored. In the present study, three common inoculum sources namely anaerobic digestion sludge (AD), pit mud (PM) and raw FW (RFW) were selected as inocula to initiate CA production from FW. The organics conversion properties, microbial community succession processes and bacterial metabolism pathways were investigated. Results showed that carbohydrates were effectively degraded into lactic acid and then to CA based on lactate-based chain elongation. The CA yield (0.37 g-COD/g-VS) using AD was higher than that inoculated with PM (0.26 g-COD/g-VS) and RFW (0.32 g-COD/g-VS). Although microbial communities in inocula were totally different, they exhibited similar succession with Firmicutes and Bacteroidetes as the dominant functional phyla. Logically, lactic acid-producing bacteria (e.g. Lactobacillus, Limosilactobacillus and Sporolactobacillus) were enriched at the early stage to prepare electron donor (lactate), and then were replaced by chain elongation bacteria for CA production. However, unclassified_Ruminococcaceae was dominant in reactor with AD, unclassified_Ruminococcaceae, Bifidobacterium, Clostridium_sensu_stricto and unclassified_Prevotellaceae were largely detected in reactors inoculated with PM and RFW, which resulted in different CA yield. This study provides useful information for caproate production from FW, and widens the knowledge of cleaner production from wastes.

己酸(CA)生产是一种很有前景的餐厨垃圾(FW)增值方法,但己酸产量低严重限制了其应用。接种源是影响微生物群落和己酸发酵过程的关键因素,但尚未得到充分探讨。本研究选择了三种常见的接种源,即厌氧消化污泥(AD)、坑泥(PM)和生FW(RFW)作为接种源,以启动FW的CA生产。研究了有机物转化特性、微生物群落演替过程和细菌代谢途径。结果表明,碳水化合物可有效降解为乳酸,然后在乳酸链延伸的基础上降解为 CA。使用 AD 的 CA 产量(0.37 g-COD/g-VS)高于接种 PM(0.26 g-COD/g-VS)和 RFW(0.32 g-COD/g-VS)的 CA 产量。虽然接种物中的微生物群落完全不同,但它们表现出相似的演替,其中以固着菌和类杆菌为主要功能门类。从逻辑上讲,乳酸生产菌(如乳酸杆菌、柠檬乳酸杆菌和孢子乳酸杆菌)在早期阶段富集以制备电子供体(乳酸),然后被链延伸菌取代以生产 CA。然而,在添加 AD 的反应器中,未分类的反刍球菌占优势;在添加 PM 和 RFW 的反应器中,未分类的反刍球菌、双歧杆菌、梭状芽孢杆菌和未分类的前梭状芽孢杆菌占优势,从而导致 CA 产量的不同。这项研究为利用 FW 生产己酸酯提供了有用的信息,并拓宽了利用废物进行清洁生产的知识面。
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引用次数: 0
A novel nCP-PVA@ACA composite with core–shell structure for efficient formaldehyde removal from air 具有核壳结构的新型 nCP-PVA@ACA 复合材料可高效去除空气中的甲醛
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114187
Removing formaldehyde from indoor environments is crucial for the health of residents. However, developing a highly efficient and cost-effective material that is safe and stable and capable of continuously removing formaldehyde from ambient air is challenging. In this study, an environmentally friendly plant composite active calcium alginate gel (nCP-PVA@ACA) was prepared by fixing slow-release nanosized calcium peroxide (nCP-PVA) and active components from cactus stems into a three-dimensional network structure of a calcium alginate gel. The microscopic morphology, chemical composition, and structure of nCP-PVA@ACA were characterized using scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction and Brunauer-Emmett-Teller. In the purification column, nCP-PVA@ACA was used as a filler, which effectively removed formaldehyde from the airflow. The results indicate that nCP-PVA was well dispersed and encapsulated by the calcium alginate gel. The formaldehyde removal efficiency of nCP-PVA@ACA ranged from 90.56 % to 98.51 % when the formaldehyde concentration in the air was in the range of 0.146–0.984 mg·m−3, with a maximum removal capacity of 89.31 mg·kg−1 (based on the dry weight of Na alginate). After 3.0 h of continuous purification, the formaldehyde concentration in the treated airflow was reduced to 0.020–0.053 mg·m−3, which was significantly lower than the recommended limit of 0.08 mg·m−3 of formaldehyde in ambient air. The synergistic effects of plant active components and slow-release nCP are key to effective formaldehyde removal. This study highlights the potential of calcium peroxide for air pollution control, providing new insights and theoretical support for their applications.
清除室内环境中的甲醛对居民的健康至关重要。然而,开发一种安全稳定、能够持续清除环境空气中甲醛的高效、高性价比材料是一项挑战。本研究将缓释纳米过氧化钙(nCP-PVA)和仙人掌茎中的活性成分固定在海藻酸钙凝胶的三维网络结构中,制备了一种环保型植物复合活性海藻酸钙凝胶(nCP-PVA@ACA)。利用扫描电子显微镜、透射电子显微镜、傅立叶变换红外光谱、X射线衍射和布鲁瑙尔-艾美特-泰勒法对nCP-PVA@ACA的微观形态、化学成分和结构进行了表征。在净化柱中,nCP-PVA@ACA 用作填充物,可有效去除气流中的甲醛。结果表明,nCP-PVA 被海藻酸钙凝胶很好地分散和包裹。当空气中的甲醛浓度在 0.146-0.984 mg-m-3 之间时,nCP-PVA@ACA 的甲醛去除率为 90.56 % 至 98.51 %,最大去除能力为 89.31 mg-kg-1(基于 Na alginate 的干重)。连续净化 3.0 小时后,处理气流中的甲醛浓度降至 0.020-0.053 mg-m-3,明显低于环境空气中甲醛的推荐限值 0.08 mg-m-3。植物活性成分和缓释 nCP 的协同作用是有效清除甲醛的关键。这项研究凸显了过氧化钙在空气污染控制方面的潜力,为其应用提供了新的见解和理论支持。
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引用次数: 0
Construction of marigold-like ZnIn2S4@Tb-g-C3N4 heterojunction for facilitating photocatalytic degradation of tetracycline and tylosin under simulated solar irradiation 构建金盏花状 ZnIn2S4@Tb-g-C3N4 异质结,促进模拟太阳辐照下四环素和泰乐菌素的光催化降解
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114175

Due to the high biological toxicity and the propensity to induce antibiotic resistance, the treatment of antibiotic wastewater has consistently posed a formidable challenge. The semiconductor photocatalysts can efficiently and completely remove antibiotics from the wastewater to repair the water environment. Therefore, a novel ZnIn2S4/Tb-g-C3N4 (ZIS/TCN) photocatalyst was successfully synthesized in this paper and its ability to efficiently degrade antibiotics has been verified. The optimized 150ZIS/TCN photocatalyst showed excellent photocatalytic performance and stablility toward the degradation of tetracycline (TC) and tylosin (TYL) under sunlight simulated with a xenon lamp. Compared with pristine g-C3N4 and ZnIn2S4, the 150ZIS/TCN exhibited superior degradation performance for TC (TYL),about 3.2 (2.1) and 1.8 (1.5) times higher than them. Based on density functional theory (DFT) calculations and experimental characterization test results, it was confirmed that the Tb doping effectively regulates the intrinsic electric field and visible light absorption capacity. This study unveils the degradation mechanism of ZIS/TCN photocatalysis and provides an effective pathway for enhancing photocatalytic degradation through rare earth doping.

由于抗生素具有较高的生物毒性和诱导抗生素耐药性的倾向,抗生素废水的处理一直是一项艰巨的挑战。半导体光催化剂可以高效、彻底地去除废水中的抗生素,修复水环境。因此,本文成功合成了一种新型 ZnIn2S4/Tb-g-C3N4 (ZIS/TCN) 光催化剂,并验证了其高效降解抗生素的能力。优化后的 150ZIS/TCN 光催化剂在氙灯模拟日光下对四环素(TC)和泰乐菌素(TYL)的降解表现出优异的光催化性能和稳定性。与原始 g-C3N4 和 ZnIn2S4 相比,150ZIS/TCN 对四环素(TC)和泰乐菌素(TYL)的降解性能更为优异,分别是它们的 3.2 (2.1) 倍和 1.8 (1.5) 倍。基于密度泛函理论(DFT)计算和实验表征测试结果,证实了掺杂 Tb 有效地调节了本征电场和可见光吸收能力。该研究揭示了 ZIS/TCN 光催化降解机理,为通过掺杂稀土提高光催化降解能力提供了有效途径。
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引用次数: 0
High selectivity syngas generation by double perovskite oxygen carriers La2Fe2-xCoxO6 for chemical looping steam methane reforming 利用双包晶载氧体 La2Fe2-xCoxO6 生成高选择性合成气,用于化学循环蒸汽甲烷转化
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114176

The generation of high-quality syngas combined with high-purity hydrogen is an essential challenge in the chemical looping steam methane reforming (CL-SMR) process, in which the design of oxygen carriers (OCs) is crucial. In this study, La2FeBO6 (BCr, Ni,Co) and La2Fe2-xCoxO6 (x = 0.2, 0.4, 0.6, 0.8, 1.0) double perovskites have been investigated as OCs in the CL-SMR process. Various analytical techniques (BET, XPS, XRD, H2-TPR, Raman.) have been deployed to characterize the OCs' specific surface area, crystal structure, and surface oxygen species. The fixed-bed experiments revealed that the Cr-modified perovskite had the lowest reactivity, which was attributed to the creation of LaCrO3 limiting the oxygen release rate of the OC. Meanwhile, Ni doping exhibited the maximum methane conversion (99.15 %), but it resulted in more carbon deposition due to methane cracking, and its carbon deposition was four times than that of Co doping. Whereas, the Co doped double perovskite OCs showed excellent overall performance, in which La2Fe1.8Co0.2O6 (L2F1.8Co0.2) exhibited the optimum CO selectivity (90.72 %), H2 selectivity (96.91 %), and H2 purity (96.84 %), as well as the lowest carbon deposition. Moreover, the L2F1.8Co0.2 also exhibited outstanding stability in 10 cycles, and it could be a prospective material for CL-SMR, enabling the simultaneous generation of high-quality syngas and high-purity hydrogen.

在化学循环蒸汽甲烷重整(CL-SMR)工艺中,生成高质量的合成气和高纯度的氢气是一个重要的挑战,其中氧载体(OCs)的设计至关重要。本研究将 La2FeBO6 (BCr, Ni, Co) 和 La2Fe2-xCoxO6 (x = 0.2, 0.4, 0.6, 0.8, 1.0) 双包晶石作为 OCs 在 CL-SMR 过程中进行了研究。采用了各种分析技术(BET、XPS、XRD、H2-TPR、拉曼)来表征 OC 的比表面积、晶体结构和表面氧物种。固定床实验表明,铬修饰的包晶具有最低的反应活性,这归因于 LaCrO3 的产生限制了 OC 的氧释放率。同时,掺杂镍的甲烷转化率最高(99.15%),但由于甲烷裂解而导致更多的碳沉积,其碳沉积量是掺杂钴的四倍。而掺杂 Co 的双包晶 OC 整体性能优异,其中 La2Fe1.8Co0.2O6(L2F1.8Co0.2)表现出最佳的 CO 选择性(90.72%)、H2 选择性(96.91%)和 H2 纯度(96.84%)以及最低的碳沉积。此外,L2F1.8Co0.2 在 10 次循环中也表现出卓越的稳定性,可作为 CL-SMR 的前瞻性材料,实现同时生成高质量的合成气和高纯度的氢气。
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引用次数: 0
Modified micro-graphite catalysed biodegradation of perchlorate and the analysis of community changes 改性微石墨催化的高氯酸盐生物降解及群落变化分析
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114189

This study investigates the effectiveness of modified micrometer graphite (MMG) in enhancing the biodegradation of perchlorate in sludge. Different MMG types, specifically GO205, GO003, ATGO205, and ATGO003, were evaluated for their impact on perchlorate degradation rates. The results showed a significant acceleration in perchlorate reduction, particularly with the MMG variant GO205, which achieved complete degradation within 48 hours, marking a six-fold increase compared to controls. This rapid degradation also correlated with enhanced microbial activity, as indicated by increased cytochrome C concentrations and electron transport system activity, suggesting a boost in overall microbial metabolic functions. Additionally, shifts in the microbial community composition were observed, with a notable increase in perchlorate-reducing bacteria populations. The study highlights MMG's potential to improve perchlorate remediation processes efficiently and offers promising insights into its application in treating perchlorate-contaminated environments.

本研究调查了改性微米石墨(MMG)在提高污泥中高氯酸盐生物降解方面的效果。研究人员评估了不同类型的 MMG(特别是 GO205、GO003、ATGO205 和 ATGO003)对高氯酸盐降解率的影响。结果表明,高氯酸盐的降解速度明显加快,尤其是 MMG 变体 GO205,在 48 小时内就实现了完全降解,比对照组提高了六倍。这种快速降解还与微生物活性的增强有关,细胞色素 C 浓度和电子传递系统活性的增加表明,微生物的整体代谢功能得到了增强。此外,还观察到微生物群落组成的变化,高氯酸盐还原菌数量明显增加。该研究强调了 MMG 有效改善高氯酸盐修复过程的潜力,并为其在处理高氯酸盐污染环境中的应用提供了前景广阔的见解。
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引用次数: 0
Pollution assessment and risk area delineation of potentially toxic elements in agricultural soils with high geological background through an integrated framework 通过综合框架对高地质背景农业土壤中的潜在有毒元素进行污染评估和风险区域划分
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114177
An integrated framework for potentially toxic elements (PTEs) pollution assessment and risk area delineation of agricultural soil in high geological background areas was developed using the western region of Guizhou Province, China, as a case study. The framework combining the finite mixture distribution model (FMDM), the influence index of comprehensive quality (IICQ), random forest (RF), geographically weighted regression (GWR) and Bayesian maximum entropy (BME) theory. The inclusion of agricultural product quality and environmental auxiliary variables in the IICQ and BEM models has enhanced the accuracy of PTEs pollution assessment and risk area delineation. The results indicated that 90.92 % of the sampled sites were at risk of PTEs pollution and showed a trend of watershed (rivers of Liuchong, Sancha and Beipan) distribution; 23.68 % of the points, at risk of heavy pollution, were mainly located in the farmland surrounding metal mining area in the upper reaches of the watershed; 18.82 % of the sites had crops exceeding the PTEs limit but no soil contamination, concentrated in the lower reaches of the watershed with low altitude and high annual average temperature. Mining and metallurgy activities, the primary risk factors causing farmland pollution, were introduced into the BME model to assist delineate pollution risk areas. The area at risk of PTEs pollution constituted 66.12 %, with heavily polluted risk areas covered 14.41 %, predominantly situated in the western and southern sectors of Bijie City, the western and northern parts of Liupanshui City, the eastern areas of Anshun City, and the northern and western regions of the Southwest Guizhou Autonomous Prefecture. The results of the study provide a reasonable assessment system for the risk delineation of PTEs contamination in arable soils in high geological background areas.
以中国贵州省西部地区为例,建立了高地质背景区农用土壤潜在有毒元素(PTEs)污染评估和风险区域划分的综合框架。该框架结合了有限混合分布模型(FMDM)、综合质量影响指数(IICQ)、随机森林(RF)、地理加权回归(GWR)和贝叶斯最大熵(BME)理论。在 IICQ 和 BEM 模型中加入农产品质量和环境辅助变量,提高了 PTEs 污染评估和风险区域划分的准确性。结果表明,90.92%的采样点位存在 PTEs 污染风险,且呈流域(六冲河、三岔河、北盘江)分布趋势;23.68%的点位存在重污染风险,主要分布在流域上游金属矿区周边农田;18.82%的点位农作物 PTEs 超标但土壤未受污染,集中分布在流域下游海拔低、年平均气温高的区域。采矿和冶金活动是造成农田污染的主要风险因素,将其引入 BME 模型有助于划定污染风险区域。PTEs 污染风险区占 66.12%,重污染风险区占 14.41%,主要分布在毕节市西部和南部、六盘水市西部和北部、安顺市东部、黔西南自治州北部和西部地区。研究结果为高地质背景地区耕地土壤中 PTEs 污染风险划分提供了合理的评估体系。
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引用次数: 0
Synergistic effect of graphdiyne (C2H2n-2) based hollow spherical Cu2O/GDY and NiS dual cocatalysts boosting photocatalytic hydrogen evolution 基于石墨二炔(C2H2n-2)的空心球形 Cu2O/GDY 和 NiS 双催化剂的协同效应可促进光催化氢气进化
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114181
The control of carrier separation morphology and efficiency is a key strategy for preparing high-performance photocatalysts. In this study, Cu2O/graphdiyne was introduced into NiS in the form of hollow nanospheres, creating a novel composite material. This method improved upon the traditional graphdiyne fabrication processes that typically use copper foil. Through the hollow spherical structure, both internal and external surface light scattering and reflection were significantly enhanced, indirectly enhancing the light absorption rate of the photocatalyst and photocatalytic activity. Ultraviolet-visible spectroscopy and photoelectrochemical results showed that using NiS as the external cocatalyst and Cu2O as the internal cocatalyst are the driving factors for the hydrogen evolution reaction, with a synergistic effect that accelerated the reaction. Such synergistic catalytic effects are rare in traditional photocatalytic systems, indicating their potential application value in enhancing catalytic efficiency. The overall performance was more than 22 times that of Cu2O/graphdiyne alone and more than 2.6 times that of NiS. Additionally, the electronic band structures and reaction mechanisms can be elucidated through Density Functional Theory (DFT) calculations, Ultraviolet Photoelectron Spectroscopy (UPS) and UV-Vis spectroscopy. These findings not only offer practical guidance but also underscore the significance of precisely manipulating the components of composite catalysts to optimize performance.
控制载体分离形态和效率是制备高性能光催化剂的关键策略。在这项研究中,Cu2O/石墨炔以空心纳米球的形式被引入 NiS,从而形成了一种新型复合材料。这种方法改进了通常使用铜箔的传统石墨二炔制造工艺。通过中空球形结构,内外表面的光散射和反射都得到了显著增强,从而间接提高了光催化剂的光吸收率和光催化活性。紫外-可见光谱和光电化学结果表明,以 NiS 为外部茧催化剂和以 Cu2O 为内部茧催化剂是氢进化反应的驱动因素,具有加速反应的协同效应。这种协同催化效应在传统光催化体系中并不多见,显示了其在提高催化效率方面的潜在应用价值。总体性能是单独使用 Cu2O/graphdiyne 的 22 倍以上,是 NiS 的 2.6 倍以上。此外,通过密度泛函理论(DFT)计算、紫外光电子能谱(UPS)和紫外可见光谱,还可以阐明电子能带结构和反应机理。这些发现不仅提供了实用指导,还强调了精确控制复合催化剂成分以优化性能的重要性。
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引用次数: 0
Construction of C3N4/Ag2S p-n semiconductor heterojunction coupled with Ag-induced SPR effect on CF cloth for improving photocatalytic activity 在 CF 布上构建 C3N4/Ag2S p-n 半导体异质结并结合 Ag 诱导的 SPR 效应以提高光催化活性
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114183

C3N4/Ag2S p-n semiconductor heterojunction coupled with Ag-induced SPR effect on carbon fiber cloth with large macroscopic area, recyclability and excellent photocatalytic performance was prepared by thermal condensation-chemical precipitation. CF/C3N4/Ag/Ag2S cloth showed strong Vis-NIR light absorption and outstanding separation efficiency of photo-generated electron and hole pairs. CF/C3N4/Ag/Ag2S cloth displayed a markedly enhanced catalytic activity (94 % of TC, 85 % of Cr(VI)) compared with CF/C3N4 cloth (52 % of TC, 50 % of Cr(VI)) or CF/Ag/Ag2S cloth (34 % of TC, 19 % of Cr(VI)), attributing to the establishment of p-n junction along with Ag SPR effect. Moreover, degradation pathways for TC were proposed utilizing HPLC-MS and Fukui index analysis, and photocatalytic mechanism was confirmed by active species experiments and DFT computations. This facile strategy provides novel approach to the synthesis of material with large macroscopic areas, recyclability, and excellent photocatalytic property for degrading contaminants from wastewater.

通过热凝结-化学沉淀法在碳纤维布上制备了具有大面积、可回收和优异光催化性能的 C3N4/Ag2S p-n 半导体异质结和 Ag 诱导的 SPR 效应。CF/C3N4/Ag/Ag2S 布具有很强的可见-近红外光吸收能力和出色的光生电子和空穴对分离效率。CF/C3N4/Ag/Ag2S 布的催化活性比 CF/C3N4 布(52% 的 TC,50% 的 Cr(VI))或 CF/Ag/Ag2S 布(34% 的 TC,19% 的 Cr(VI))明显提高(94% 的 TC,85% 的 Cr(VI)),这归功于 p-n 结的建立和 Ag SPR 效应。此外,还利用 HPLC-MS 和福井指数分析提出了三氯甲烷的降解途径,并通过活性物种实验和 DFT 计算证实了光催化机理。这种简便的策略为合成具有大面积、可回收和优异光催化性能的材料提供了新方法,可用于降解废水中的污染物。
{"title":"Construction of C3N4/Ag2S p-n semiconductor heterojunction coupled with Ag-induced SPR effect on CF cloth for improving photocatalytic activity","authors":"","doi":"10.1016/j.jece.2024.114183","DOIUrl":"10.1016/j.jece.2024.114183","url":null,"abstract":"<div><p>C<sub>3</sub>N<sub>4</sub>/Ag<sub>2</sub>S p-n semiconductor heterojunction coupled with Ag-induced SPR effect on carbon fiber cloth with large macroscopic area, recyclability and excellent photocatalytic performance was prepared by thermal condensation-chemical precipitation. CF/C<sub>3</sub>N<sub>4</sub>/Ag/Ag<sub>2</sub>S cloth showed strong Vis-NIR light absorption and outstanding separation efficiency of photo-generated electron and hole pairs. CF/C<sub>3</sub>N<sub>4</sub>/Ag/Ag<sub>2</sub>S cloth displayed a markedly enhanced catalytic activity (94 % of TC, 85 % of Cr(VI)) compared with CF/C<sub>3</sub>N<sub>4</sub> cloth (52 % of TC, 50 % of Cr(VI)) or CF/Ag/Ag<sub>2</sub>S cloth (34 % of TC, 19 % of Cr(VI)), attributing to the establishment of p-n junction along with Ag SPR effect. Moreover, degradation pathways for TC were proposed utilizing HPLC-MS and Fukui index analysis, and photocatalytic mechanism was confirmed by active species experiments and DFT computations. This facile strategy provides novel approach to the synthesis of material with large macroscopic areas, recyclability, and excellent photocatalytic property for degrading contaminants from wastewater.</p></div>","PeriodicalId":15759,"journal":{"name":"Journal of Environmental Chemical Engineering","volume":null,"pages":null},"PeriodicalIF":7.4,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142271589","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
Continuous oxidation of organic contaminates in soil by polylactic acid-coated KMnO4 聚乳酸包覆 KMnO4 对土壤中有机污染物的持续氧化作用
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114154
Potassium permanganate (KMnO4), as a versatile and safe solid source of MnO4-, received substantial attention from researchers as a potential soil oxidant reagent. In this study, we prepared polylactic acid (PLA)-coated KMnO4 (KMnO4@PLA) to control MnO4- release. The experimental results indicated that the optimal preparation scheme for KMnO4@PLA was a particle size of 1–2 mm, a solid-liquid ratio of 1:3, and a core-shell ratio of 1:3. And the release lifetimes of MnO4- from KMnO4@PLA in aqueous and quartz sand media were 200 hours and 310 hours, respectively, which were 2400 and 33 times longer than the release lifetimes of raw KMnO4. The controlled release of MnO4- from KMnO4@PLA was achieved through the hydrolysis of PLA. And the release process adhered to first-order reaction kinetics and displayed Fickian diffusion characteristics. Moreover, the removal of phenol by KMnO4@PLA in aqueous, quartz sand, and soil media were investigated through batch and flow column experiments. Compared with the raw KMnO4, the KMnO4@PLA exhibited a stronger ability to degrade phenol, due to the mildly acidic nature of the PLA shell. These findings demonstrated that KMnO4@PLA has significant advantages for the remediation of organically contaminated soils.
高锰酸钾(KMnO4)是一种多功能、安全的固体氧化锰来源,作为一种潜在的土壤氧化剂试剂受到了研究人员的广泛关注。在本研究中,我们制备了聚乳酸(PLA)包覆的 KMnO4(KMnO4@PLA)来控制 MnO4- 的释放。实验结果表明,KMnO4@PLA 的最佳制备方案为粒径 1-2 mm、固液比 1:3、核壳比 1:3。KMnO4@PLA在水介质和石英砂介质中的MnO4-释放寿命分别为200小时和310小时,分别是未加工KMnO4释放寿命的2400倍和33倍。KMnO4@PLA 中 MnO4- 的控释是通过聚乳酸的水解实现的。释放过程符合一阶反应动力学,并表现出菲氏扩散特性。此外,还通过间歇实验和流柱实验研究了 KMnO4@PLA 在水介质、石英砂介质和土壤介质中对苯酚的去除效果。与未加工的 KMnO4 相比,由于聚乳酸外壳呈弱酸性,KMnO4@PLA 对苯酚的降解能力更强。这些研究结果表明,KMnO4@PLA 在修复受有机物污染的土壤方面具有显著优势。
{"title":"Continuous oxidation of organic contaminates in soil by polylactic acid-coated KMnO4","authors":"","doi":"10.1016/j.jece.2024.114154","DOIUrl":"10.1016/j.jece.2024.114154","url":null,"abstract":"<div><div>Potassium permanganate (KMnO<sub>4</sub>), as a versatile and safe solid source of MnO<sub>4</sub><sup>-</sup>, received substantial attention from researchers as a potential soil oxidant reagent. In this study, we prepared polylactic acid (PLA)-coated KMnO<sub>4</sub> (KMnO<sub>4</sub>@PLA) to control MnO<sub>4</sub><sup>-</sup> release. The experimental results indicated that the optimal preparation scheme for KMnO<sub>4</sub>@PLA was a particle size of 1–2 mm, a solid-liquid ratio of 1:3, and a core-shell ratio of 1:3. And the release lifetimes of MnO<sub>4</sub><sup>-</sup> from KMnO<sub>4</sub>@PLA in aqueous and quartz sand media were 200 hours and 310 hours, respectively, which were 2400 and 33 times longer than the release lifetimes of raw KMnO<sub>4</sub>. The controlled release of MnO<sub>4</sub><sup>-</sup> from KMnO<sub>4</sub>@PLA was achieved through the hydrolysis of PLA. And the release process adhered to first-order reaction kinetics and displayed Fickian diffusion characteristics. Moreover, the removal of phenol by KMnO<sub>4</sub>@PLA in aqueous, quartz sand, and soil media were investigated through batch and flow column experiments. Compared with the raw KMnO<sub>4</sub>, the KMnO<sub>4</sub>@PLA exhibited a stronger ability to degrade phenol, due to the mildly acidic nature of the PLA shell. These findings demonstrated that KMnO<sub>4</sub>@PLA has significant advantages for the remediation of organically contaminated soils.</div></div>","PeriodicalId":15759,"journal":{"name":"Journal of Environmental Chemical Engineering","volume":null,"pages":null},"PeriodicalIF":7.4,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142323881","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
Microwave solvothermal synthesis of high entropy oxide on carbon nanotubes towards high-performance lithium-ion battery anode 微波溶热合成碳纳米管上的高熵氧化物,实现高性能锂离子电池负极
IF 7.4 2区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2024-09-18 DOI: 10.1016/j.jece.2024.114085
Transition metal oxide (TMO) anodes with multielectron transfer mechanism exhibit high theoretical capacity for lithium-ion batteries. However, the huge volume changes of TMOs during the lithiation/delithiation process limit their commercialization. High entropy oxides (HEOs) with unique component and structure adjustability demonstrate attractive lithium storage potential. While the inherently poor electrical conductivity of oxides remains a problem. Herein, the amorphous HEOs grown in situ on the surface of carbon nanotubes (CNTs) through simple and rapid microwave solvothermal method followed by heat treatment. The composite shows high capacity and excellent cycle and rate performance. The HEO@CNT-60 with an optimal amount of CNTs added maintains a specific capacity of 560.1 mAh g−1 after 500 cycles at a current density of 1 A g−1 with the capacity retention rate of 86.4 %. The improved charge transfer kinetics and Li+ diffusion rate together with the pseudocapacitance contributions are the main reason for the excellent electrochemical performance, which is related with the uniformly dispersed nanoscale active materials, the entropy stabilization mechanism, the synergistic effect of multiple transition metal elements and abundant oxygen vacancies, the good electrical conductivity of CNTs, and the tight heterogeneous interfaces between HEOs and CNTs. This report suggests a strategy to further exploit the lithium storage potential of high entropy oxides.
具有多电子转移机制的过渡金属氧化物(TMO)阳极在锂离子电池中具有很高的理论容量。然而,TMO 在锂化/退锂过程中的巨大体积变化限制了其商业化。具有独特成分和结构可调性的高熵氧化物(HEOs)展现了极具吸引力的锂存储潜力。但氧化物固有的不良导电性仍然是一个问题。在这里,通过简单快速的微波溶热法,在碳纳米管(CNT)表面原位生长出非晶态高熵氧化物,然后进行热处理。该复合材料具有高容量、优异的循环和速率性能。添加了最佳量 CNT 的 HEO@CNT-60 在电流密度为 1 A g-1 的条件下循环 500 次后,比容量仍为 560.1 mAh g-1,容量保持率为 86.4%。电荷转移动力学和 Li+ 扩散速率的改善以及假电容贡献是其优异电化学性能的主要原因,这与均匀分散的纳米级活性材料、熵稳定机制、多种过渡金属元素和丰富氧空位的协同效应、CNT 的良好导电性以及 HEOs 和 CNT 之间紧密的异质界面有关。本报告提出了进一步开发高熵氧化物锂存储潜力的策略。
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Journal of Environmental Chemical Engineering
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