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Impact of WO3:CeO2@MXene/gC3N4 nano disk on sunlight-driven photocatalytic removal of fluoroquinolone antibiotic and high-performance supercapacitor application WO3:CeO2@MXene/gC3N4纳米片对光催化去除氟喹诺酮类抗生素及高性能超级电容器应用的影响
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-07-21 DOI: 10.1007/s42823-025-00951-1
Rubesh Ashok Kumar Selvakumar, Vasvini Mary Devaraj, Rachel Angeline Lenin, Nagarani Sandran, Jih-Hsing Chang, Suganya Josephine Gali Anthoni

This research highlights the use of a WO3:CeO2@MXene/gC3N4 (MGWC) nanodisk as a versatile material. MGWC demonstrates efficient photocatalytic degradation of moxifloxacin (MOF) in water under sunlight and also shows great promise for high-performance supercapacitor applications. MGWC was synthesized using a modified hydrothermal method and thoroughly characterized using various techniques. The MGWC showed a band gap energy of 2.79 eV determined through UV–Vis DRS analysis and an average crystallite size of 39.6 nm calculated from XRD. A promising photocatalytic activity was observed for the degradation of MOF, outperforming other photocatalysts. Additionally, preliminary studies examined variations in catalyst concentration, pH, kinetics, electrolytes, scavengers, reusability, and TOC, contributing valuable insights. Under optimal conditions, the MOF achieved almost complete degradation, reaching about 99.7% within 180 min using the MGWC photocatalyst. Additionally, MGWC exhibits promising potential in supercapacitor applications. EIS and CV studies have been used to examine MGWC’s exceptional charge transfer properties. CV tests confirm the pseudo-capacitive nature of MGWC electrodes. GCD studies of MGWC exhibit a high specific capacitance of 551 F/g at 1 A/g with incomparable capacitance retention of 98.1% over 10,000 cycles. This research not only aids in reducing emerging environmental pollutants but also sets the stage for sustainable energy solutions.

这项研究强调了WO3:CeO2@MXene/gC3N4 (MGWC)纳米盘作为一种通用材料的使用。MGWC在阳光下对水中的莫西沙星(MOF)进行了有效的光催化降解,在高性能超级电容器方面也有很大的应用前景。采用改进的水热法合成了MGWC,并采用各种技术对其进行了表征。通过UV-Vis DRS分析,MGWC的能带能为2.79 eV, XRD计算的平均晶粒尺寸为39.6 nm。MOF的光催化性能优于其他光催化剂。此外,初步研究考察了催化剂浓度、pH值、动力学、电解质、清除剂、可重用性和TOC的变化,提供了有价值的见解。在最佳条件下,使用MGWC光催化剂,MOF在180 min内几乎完全降解,达到99.7%左右。此外,MGWC在超级电容器应用中也显示出很大的潜力。EIS和CV研究已经被用来检验MGWC的特殊电荷转移特性。CV试验证实了MGWC电极的伪电容性。GCD研究表明,MGWC在1 a /g时具有551 F/g的高比电容,在10,000次循环中具有98.1%的无与伦比的电容保持率。这项研究不仅有助于减少新出现的环境污染物,而且为可持续能源解决方案奠定了基础。
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引用次数: 0
Water-oxidized and ball-milled reduced graphene oxide based self-supporting electrodes for high performance flexible supercapacitors 用于高性能柔性超级电容器的水氧化和球磨还原氧化石墨烯自支撑电极
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-07-20 DOI: 10.1007/s42823-025-00950-2
Jae Young Jung, Dong-gun Kim, Sungkwon Jung, Sujin Kim, Jae-yeong Kang, Yong-seong Park, Hongbum Kim, Nam Dong Kim, Pil Kim

With the increasing demand for flexible electronic devices, smaller and lighter flexible supercapacitors have gained significant research attention. Among the various materials, self-supporting reduced graphene oxide (rGO) paper has emerged as one of the most promising electrode materials for supercapacitors due to its low cost, high chemical/thermal stability, and excellent electrical conductivity. Nevertheless, a major drawback of rGO paper is the limited ion diffusion between stacked rGO layers, hindering the effective formation of electrochemical double-layer at the electrode/electrolyte interface. In this study, we prepared the rGO paper derived from ball-milled followed-by water oxidation process for reducing the sheet size. The smaller-sized rGO sheets facilitated ion transport between graphene layers, promoting efficient electric double-layer formation. Moreover, the increased presence of edge planes in ball-milled rGO sheets achieved high capacitance, further enhancing the performance of rGO as an electrode material. Notably, the 2-BMOX rGO paper obtained from ball-milling and wet-oxidized graphite exhibited a capacitance of 117.9 F/g in cyclic voltammetry (CV) and 128.6 F/g in galvanostatic charge–discharge (GCD) tests, approximately twice that of conventional rGO. Additionally, the capacitance retained 91% of its initial performance after 2,000 cycles, indicating excellent cycling stability.

随着人们对柔性电子器件需求的不断增加,体积更小、重量更轻的柔性超级电容器受到了人们的广泛关注。在各种材料中,自支撑还原性氧化石墨烯(rGO)纸因其成本低、化学/热稳定性高、导电性好等优点,已成为超级电容器极具应用前景的材料之一。然而,还原氧化石墨烯纸的一个主要缺点是堆积的还原氧化石墨烯层之间的离子扩散有限,阻碍了电极/电解质界面上电化学双层的有效形成。在本研究中,我们制备了由球磨后水氧化工艺得到的还原氧化石墨烯纸,以减小纸张尺寸。较小尺寸的氧化石墨烯薄片促进了石墨烯层之间的离子传输,促进了高效的双电层形成。此外,球磨氧化石墨烯薄片中边缘平面的增加实现了高电容,进一步提高了氧化石墨烯作为电极材料的性能。值得注意的是,通过球磨和湿氧化石墨制备的2-BMOX还原氧化石墨纸在循环伏安(CV)和恒流充放电(GCD)测试中表现出117.9 F/g和128.6 F/g的电容,大约是常规还原氧化石墨烯的两倍。此外,在2000次循环后,电容保持了91%的初始性能,表明了出色的循环稳定性。
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引用次数: 0
Self-supporting laser-induced graphene-based electrodes for efficient OER and 5-hydroxymethylfurfural oxidation 用于高效OER和5-羟甲基糠醛氧化的自支持型激光诱导石墨烯电极
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-07-18 DOI: 10.1007/s42823-025-00948-w
Xinyu Xiao, Mingyue Li, Guangmeng Chen, Weihua Zhou, Weiwei Zhao, Xiaoqing Liu

Improving the oxygen evolution reaction (OER) performance or replacing OER with the value-added conversion of biomass is of great significance for the green hydrogen energy production. In this work, bimetallic species-decorated laser-induced graphene (LIG) was fabricated and demonstrated as the self-supported electrodes towards efficient OER and 5-hydroxymethylfurfural oxidation reaction (HMFOR). Three-dimensional LIG was obtained via one-step irradiation process under ambient conditions, and active metal species were then introduced through electrodeposition, with Ni-based catalyst as the primary catalytic material and Fe and Co as modified metals. Among, LIG-NiFe electrode achieved an extremely low overpotential of 241.7 mV at a current density of 20 mA/cm2 for OER and demonstrated long-term stability. This could be attributed to the promoted formation of Ni3+ active centers by Fe modified and the intrinsic porous structure of LIG providing an enhanced surface area. As for LIG-NiCo, due to the low onset potential of Co for HMF, it could achieve 99.6% HMF conversion and yielded value-added 2, 5-furandicarboxylic acid (FDCA) with a selectivity of 87.1%. Coupled with the merit of facile fabrication of LIG framework, this study demonstrates that LIG-based electrodes assume great practical application value in electrocatalytic reactions.

Graphical abstract

提高析氧反应(OER)性能或用生物质的增值转化替代OER对绿色氢能源生产具有重要意义。在这项工作中,制备了双金属物种修饰的激光诱导石墨烯(LIG),并证明了其作为高效OER和5-羟甲基糠醛氧化反应(HMFOR)的自支撑电极。采用常温下一步辐照法制备三维LIG,以ni基催化剂为一级催化材料,Fe和Co为改性金属,通过电沉积法引入活性金属。其中,在电流密度为20 mA/cm2时,li - nife电极的过电位极低,为241.7 mV,且具有长期稳定性。这可能是由于Fe修饰促进了Ni3+活性中心的形成,以及LIG固有的多孔结构提供了增强的表面积。对于ligo - nico,由于Co对HMF的起效电位较低,可以实现99.6%的HMF转化率,并产生选择性为87.1%的增值型2,5 -呋喃二羧酸(FDCA)。再加上LIG框架易于制作的优点,本研究证明了基于LIG的电极在电催化反应中具有很大的实际应用价值。图形抽象
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引用次数: 0
Facile synthesis of activated carbon/copper/copper oxide composite electrode material for supercapacitors using C.I. Pigment Blue 15:3 C.I.颜料蓝15:3快速合成超级电容器用活性炭/铜/氧化铜复合电极材料
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-07-14 DOI: 10.1007/s42823-025-00949-9
Gunhwan Park, Woong Kwon, Jiyeon Cheon, Daeun Kim, Gyeongjin Kim, Euigyung Jeong

In this study, C.I. Pigment Blue 15:3, an organic phthalocyanine based pigment, was used as a precursor to synthesize activated carbon/copper/copper oxide composite through a carbonization and activation process. The resulting composite was investigated to evaluate the potential use as a hybrid capacitor electrode of supercapacitor and pseudo-capacitor. Precursor was pre-treated at 600 °C, followed by activation at 750 °C using alkaline activating agents (KOH and K2CO3). Neutral ZnCl2 activating agent was also used for activation at 700 °C without pre-treatment to compare the electrochemical performance. The KOH activated sample exhibited the presence of Cu, CuO, and Cu2O in XRD and XPS analysis results and it also showed a highest specific surface area of 2731 m2/g and well-developed 0.7–2.0 nm micropores, enhancing ion adsorption in K2SO4 electrolyte. Electrochemical tests revealed that PB_KOH exhibited the highest capacitance, outperforming commercial Norit Carbon at various current densities, due to its Cu/CuO/Cu2O/activated carbon composite structure. These findings highlight its strong potential as a high-performance supercapacitor electrode material.

本研究以有机酞菁颜料C.I.色素蓝15:3为前驱体,通过炭化活化工艺合成活性炭/铜/氧化铜复合材料。研究了复合材料作为超级电容器和伪电容器混合电容器电极的潜在用途。前驱体在600℃下进行预处理,然后在750℃下使用碱性活化剂(KOH和K2CO3)活化。采用中性ZnCl2活化剂在700℃下进行活化,不进行预处理,比较电化学性能。XRD和XPS分析结果表明,KOH活化后的样品存在Cu、CuO和Cu2O,具有2731 m2/g的最高比表面积和发育良好的0.7 ~ 2.0 nm微孔,有利于离子在K2SO4电解质中的吸附。电化学测试表明,PB_KOH由于其Cu/CuO/Cu2O/活性炭复合结构,在各种电流密度下均表现出最高的电容,优于商用Norit炭。这些发现突出了其作为高性能超级电容器电极材料的强大潜力。
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引用次数: 0
Synthesis and application of single-walled carbon nanotube 单壁碳纳米管的合成与应用
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-07-13 DOI: 10.1007/s42823-025-00946-y
Qianpeng Dong, Peng Wang, Chenyu Gao, Rongfeng Jiang, Yan Li, Dianming Chu, Wenjuan Bai, Yan He

Single-walled carbon nanotubes (SWCNTs) are a promising material for advancing the field of materials. However, controlling the controlled growth of SWCNTs by conventional chemical vapor deposition or other growth processes remains challenging. Recent studies have shown that some progress has been made in the synthesis mechanism, catalysts and growth processes of SWCNTs, which makes the controlled growth of SWCNTs possible. This paper reviews the common SWCNTs, the synthesis process, and the applications. The paper firstly discusses the differences in the structure and properties of different types of SWCNTs and the related studies on these properties. Next, the paper discusses the mechanisms, catalysts, and growth processes used to synthesize SWCNTs, from experimental characterization to simulation analysis. Subsequently, the paper describes some applications of SWCNTs in popular fields such as functionalization, transistors, electrochemistry, and so on. Finally, a brief outlook on the challenges and future development of these SWCNTs in the research field is presented.

单壁碳纳米管(SWCNTs)是一种极具发展前景的材料。然而,通过传统的化学气相沉积或其他生长工艺来控制SWCNTs的可控生长仍然具有挑战性。近年来的研究表明,在SWCNTs的合成机理、催化剂和生长过程等方面取得了一定进展,使SWCNTs的可控生长成为可能。本文综述了常见的SWCNTs及其合成方法和应用。本文首先讨论了不同类型SWCNTs在结构和性能上的差异以及对这些性能的相关研究。接下来,本文讨论了SWCNTs合成的机理、催化剂和生长过程,从实验表征到模拟分析。随后介绍了SWCNTs在功能化、晶体管、电化学等热门领域的一些应用。最后,对这些SWCNTs在研究领域面临的挑战和未来发展进行了简要展望。
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引用次数: 0
Controlling the softening point of mesophase pitch via edge-selective fluorination 采用边缘选择性氟化技术控制中间相沥青软化点
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-07-12 DOI: 10.1007/s42823-025-00947-x
Chaehun Lim, ·Seongjae Myeong, ·Sangyeop Lee, ·Seongmin Ha, Young-Seak Lee

Modifying the softening point (SP) of pitch is crucial owing to its substantial influence on pitch applicability. This study presents a novel fluorination technique for engineering the SP of mesophase pitch (MP). Low-concentration fluorine gas was used to modify the edge sites of the MP, allowing for either an increase or decrease in the SP by controlling the gas reactivity. The fluorination was conducted with 20 vol% F2 gas under reaction temperature of 25, 50, and 75 ℃ for 2 h in atmospheric pressure. A reduction in SP was achieved through edge alkylation, with a decrease of up to 14.1% observed after the fluorination. Conversely, an increase in SP resulted from edge dealkylation at higher reaction temperatures. As the modified MPs retained perfect anisotropy, this study offers an effective strategy for adjusting the SP to meet application needs without causing structural deterioration.

沥青软化点对沥青的适用性有重要影响,因此对其进行改性至关重要。本研究提出了一种用于中间相沥青(MP) SP工程的新型氟化技术。使用低浓度氟气体来修饰MP的边缘位置,通过控制气体反应性来增加或减少SP。在常压下,在25、50、75℃的反应温度下,用20 vol% F2气体氟化2 h。SP的减少是通过边缘烷基化实现的,氟化后观察到SP的减少高达14.1%。相反,在较高的反应温度下,边缘脱烷基会导致SP的增加。由于改进的MPs保留了完美的各向异性,本研究提供了有效的策略来调整SP以满足应用需求,而不会造成结构恶化。
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引用次数: 0
B, S doped zero-dimensional carbon quantum dots from bio-waste for high density supercapacitors 生物废弃物中掺杂B、S的零维碳量子点用于高密度超级电容器
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-07-10 DOI: 10.1007/s42823-025-00945-z
Suman, Gita Rani,  Bhawna, Harish Kumar, Jai Devi,  Siddharth

Double-layer supercapacitors (SCs) based on carbon quantum dots (CQDs) are a novel and highly potential electrical energy storage technology. They have a high-power density (Pd) and a long span life, which are desirable for electric automobiles, however, their specific capacitance (Csp) needs to be improved. Here, we introduce an affordable and environmentally sustainable method to enhance the capacitance of Boron-Sulphur doped carbon quantum dots (B,S-CQDs) from Oloptum miliaceum (Grass) via the hydrothermal method. The findings show that heteroatom-doping might greatly enhance the Csp and energy density (Ed) when compared to undoped CQDs. As a consequence, the B,S-CQDs demonstrate a high Csp of 390 F g−1 at 0.1 A g−1 and 152 F g−1 at 1.0 A g−1, revealing excellent rate performance. Along with the electrode demonstrates superb coulombic efficiency with only 2% efficiency loss after 3000 cycles. Furthermore, the B,S-CQDs with a wide voltage range of 0.8 V yields a remarkable Ed of 48.0 Wh kg−1 and Pd of 524 W kg−1. These promising findings demonstrate an economical and environmentally friendly electrode material for high-performance SCs. This study offers ideas for the design and preparation of SCs electrode materials and represents a major endeavour to turn waste biomass (smilograss) into a useful electrode material.

基于碳量子点(CQDs)的双层超级电容器(SCs)是一种新型的、极具潜力的储能技术。它们具有电动汽车所需要的高功率密度(Pd)和长寿命,但其比电容(Csp)需要提高。本文介绍了一种经济实惠且环境可持续的方法,通过水热法增强硼硫掺杂碳量子点(B,S-CQDs)的电容。结果表明,与未掺杂的CQDs相比,杂原子掺杂可以显著提高Csp和能量密度(Ed)。因此,B,S-CQDs在0.1 a g−1和1.0 a g−1下的Csp值分别为390 F g−1和152 F g−1,显示出优异的速率性能。同时,该电极在3000次循环后的库仑效率仅为2%。此外,在0.8 V宽电压范围下,B,S-CQDs的Ed为48.0 Wh kg - 1, Pd为524 W kg - 1。这些有希望的发现证明了一种经济环保的高性能sc电极材料。该研究为SCs电极材料的设计和制备提供了思路,代表了将废弃生物质(剑草)转化为有用电极材料的重大努力。
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引用次数: 0
Machine learning-based carbon emission prediction and influence factor analysis discussion in China cement industry 基于机器学习的中国水泥行业碳排放预测及影响因素分析探讨
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-07-10 DOI: 10.1007/s42823-025-00944-0
Chao-qiang Wang, An-ping Zuo, Yan-yan Liu

Based on a carbon emission inventory of China’s cement industry, this study evaluates the performance of six machine learning models—ridge regression (RR), polynomial regression (PR), random forest (RF), support vector machine (SVR), gradient boosted regression tree (GBRT), and feed-forward neural network (FNN)—in predicting carbon emissions. Model accuracy, feature importance, and residual distributions were analyzed. Results show that clinker production and coal consumption are the dominant factors, contributing 83.7% and 11.95% to emissions, respectively. PR and FNN achieved the best performance with R2 values up to 0.99 and lowest mean square errors (0.11 and 1.82). Their mechanisms were further adapted to improve the generalization of other models. Spatial analysis revealed that North, South, and Southwest China are major emission regions. Using the optimal model, emissions in 2035 are projected to reach 519.14 million tonnes. This study offers technical insights for model optimization and supports low-carbon policymaking in the cement industry.

基于中国水泥行业的碳排放清单,本研究评估了六种机器学习模型——脊回归(RR)、多项式回归(PR)、随机森林(RF)、支持向量机(SVR)、梯度增强回归树(GBRT)和前馈神经网络(FNN)——在预测碳排放方面的性能。分析了模型精度、特征重要性和残差分布。结果表明,熟料生产和煤炭消耗是主导因素,对排放的贡献率分别为83.7%和11.95%。PR和FNN表现最佳,R2值可达0.99,均方误差最小(0.11和1.82)。它们的机制被进一步调整,以提高其他模型的通用性。空间分析表明,华北、华南和西南是主要的排放区。使用最优模型,2035年的排放量预计将达到5.1914亿吨。该研究为模型优化提供了技术见解,并为水泥行业的低碳政策制定提供了支持。
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引用次数: 0
Sodium-induced phase shift in α-NaMnO2 and electrochemical properties of the full cells using hard carbon anodes derived from regional olive leaves 钠诱导α-NaMnO2的相移和采用橄榄叶硬碳阳极制备的全电池的电化学性能
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-07-05 DOI: 10.1007/s42823-025-00942-2
Ebru Dogan, Sibel Ozcan, Canan Aksu Canbay, Mesut Karta, Tolga Depci, Serdar Altin

In this study, we investigated the effect of excess sodium (Na) in a NaMnO2 structure using one-step heat treatment at 900 °C followed by quenching in liquid nitrogen (N₂). According to the X-ray diffraction (XRD) analysis, there was a competition between the monoclinic and orthorhombic phases, and we found that there were two monoclinic phases with similar structural properties. Therefore, we focused on revealing the formation of two isostructures of the monoclinic phase triggered by Na ions. We found that the lattice parameters and β angle changed from 113° to 105° in the samples with increasing Na content. Structural analysis of the powders using the XRD data was conducted using Rietveld refinement, and the phase ratios for all samples were calculated. The sample with x = 1.3 showed a 95% α-phase. To understand the formation of the two isostructures, we performed Density functional theory (DFT) calculations to examine their band structure, stability, and formation energy. A structural analysis of the excess Na-doped samples was performed using common techniques, and it was found that excess Na caused the formation of a coating on the grains in the form of sodium oxide. To validate this prediction, we conducted inductively coupled plasma mass spectrometry (ICP-MS), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy coupled with energy dispersive X-ray (SEM–EDX) analyses using the basic properties of these techniques and their interactions with materials. In the second part of the study, we produced HC from locally sourced olive leaves and investigated their structural properties. The electrochemical properties of the electrode materials were examined using a half-cell configuration as electrodes with Na metal and a full-cell configuration using x = 1.3 cathode and HC anode. A direct-contact pre-sodiation strategy was used as the anode in the full-cell measurements. It was found that the full cells had initial capacity values of 150 mAh/g for the voltage range 1.5–4.3 V and 120 mAh/g for the voltage range 1.5–3.5 V.

在这项研究中,我们研究了过量钠(Na)在NaMnO2结构中的影响,采用900°C一步热处理,然后在液氮(n2)中淬火。根据x射线衍射(XRD)分析,单斜相和正交相之间存在竞争,我们发现有两种结构性质相似的单斜相。因此,我们的重点是揭示由Na离子引发的单斜相的两种同工结构的形成。随着Na含量的增加,样品的晶格参数和β角从113°变化到105°。采用Rietveld细化法对粉末的XRD数据进行了结构分析,并计算了各样品的相比。当x = 1.3时,样品为95% α相。为了了解这两种同工结构的形成,我们进行了密度泛函理论(DFT)计算,以检查它们的能带结构、稳定性和形成能。利用常规技术对过量掺钠样品进行了结构分析,发现过量的Na导致晶粒上以氧化钠的形式形成涂层。为了验证这一预测,我们利用这些技术的基本特性及其与材料的相互作用,进行了电感耦合等离子体质谱(ICP-MS)、x射线光电子能谱(XPS)和扫描电子显微镜耦合能量色散x射线(SEM-EDX)分析。在研究的第二部分,我们从当地的橄榄叶中生产HC,并研究了它们的结构特性。电极材料的电化学性能分别采用半电池结构和全电池结构,分别采用金属钠作为电极和x = 1.3阴极和HC阳极。在全电池测量中,采用直接接触预钠化策略作为阳极。研究发现,在1.5-4.3 V电压范围内,完整电池的初始容量值为150 mAh/g,在1.5-3.5 V电压范围内,初始容量值为120 mAh/g。
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引用次数: 0
Simulation of microwave heating characteristics of activated carbon 活性炭微波加热特性的模拟
IF 5.8 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-30 DOI: 10.1007/s42823-025-00928-0
Yulei Qiao, Hang Chen, Sihan Liu, Anqi Xia, Yeshun Tian, Changliang Wu, Xiuzhi Zhang, Shuxia Feng, Xiao Xia, Liqiang Zhang, Guangbin Duan

To explore the heating characteristics of activated carbon in a microwave field, the effects of microwave irradiation power, the radius and physical properties of activated carbon, and a symmetrical waveguide on the heating characteristics of activated carbon in a microwave field were studied by experiments and simulation. This study distinguishes itself from previous works by focusing on high-power microwave heating (up to 800 W) and providing a comprehensive analysis of key parameters such as radius, thermal conductivity, magnetic conductivity, and dielectric constant. Additionally, the use of symmetrical waveguides and their impact on heating efficiency represents a novel contribution to the field of microwave-assisted flue gas desulfurization. According to the results, with the increase in microwave irradiation power, the heating rate of activated carbon in the microwave field increases, and the final temperature also rises. Waveguides significantly influence the heating characteristics of activated carbon. When multiple waveguides act on the same microwave field, electromagnetic waves interfere with each other and affect the distribution and intensity of the electromagnetic field. With an increase in the imaginary part of the relative permittivity, the real part of the relative magnetic permeability, and the thermal conductivity of the heated material, the heating characteristics of activated carbon in the microwave field are improved. This study provides a theoretical model for the heating characteristics and temperature distribution of activated carbon in a microwave field under high irradiation power.

为了探究活性炭在微波场中的加热特性,通过实验和模拟研究了微波辐照功率、活性炭的半径和物理性质以及对称波导对活性炭在微波场中的加热特性的影响。与以往的研究不同,本研究的重点是高功率微波加热(高达800w),并提供了半径、导热系数、导电性和介电常数等关键参数的综合分析。此外,对称波导的使用及其对加热效率的影响为微波辅助烟气脱硫领域做出了新的贡献。结果表明,随着微波辐照功率的增大,活性炭在微波场中的升温速率增大,最终温度也随之升高。波导对活性炭的加热特性有显著影响。当多个波导作用于同一个微波场时,电磁波相互干扰,影响电磁场的分布和强度。随着被加热材料相对介电常数的虚部、相对磁导率的实部和导热系数的增大,活性炭在微波场中的加热特性得到改善。本研究为高辐照功率微波场下活性炭的加热特性和温度分布提供了理论模型。
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引用次数: 0
期刊
Carbon Letters
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