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Efficient activation of N and S co-doped magnetic biochar for peroxomonosulfate degradation of tetracycline 高效活化 N 和 S 共掺磁性生物炭,促进过硫酸单胞菌降解四环素
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-09-15 DOI: 10.1002/apj.3156
Xi Zhang, Haoyuan Zheng, Hong Xu, Jie Huang, Qianyuan Mo, Guishang Sheng
N-S co-doped magnetic biochar (NSMBC) was synthesized by a two-step pyrolysis technique and used for the degradation of tetracycline (TC) by activated persulfate (peroxomonosulfate [PMS]). Batch experiments showed that the pyrolysis temperature and doping ratio affected the catalytic performance of NSMBC. The degradation rate of TC in the NSMBC/PMS system prepared at 350°C with a doping ratio of 33% was up to 94.50%, and the system exhibited strong pH adaptability and resistance to environmental interference. The results of free radical burst and electron paramagnetic resonance (EPR) spectroscopy experiments indicated the free radical pathway (SO4•−) for TC degradation. In addition, NSMBC has good stability and excellent magnetic properties favorable for separation and recovery. This study not only provides a new idea for the synthesis of efficient and stable catalysts but also provides a green pathway for the resourceization of pomelo peel waste.
通过两步热解技术合成了 N-S 共掺杂磁性生物炭(NSMBC),并将其用于活化过硫酸盐(过硫酸单胞菌 [PMS])降解四环素(TC)。批量实验结果表明,热解温度和掺杂率会影响 NSMBC 的催化性能。掺杂比为 33% 的 NSMBC/PMS 体系在 350°C 下的 TC 降解率高达 94.50%,且该体系具有较强的 pH 适应性和抗环境干扰能力。自由基猝灭和电子顺磁共振(EPR)光谱实验结果表明,自由基(SO4--)是降解 TC 的途径。此外,NSMBC 具有良好的稳定性和优异的磁性,有利于分离和回收。这项研究不仅为合成高效稳定的催化剂提供了新思路,也为柚子皮废弃物的资源化提供了一条绿色通道。
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引用次数: 0
Sulfonated carbon–based heterogeneous acid catalysts in direct biomass redox flow fuel cell: A review 直接生物质氧化还原流燃料电池中的磺化碳基异质酸催化剂:综述
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-09-14 DOI: 10.1002/apj.3158
Boniface Ifeanyi Ugwu, Christogonus Oduney Akalezi, Innocent Sunday Ike, Toochukwu Eqwutosi Ogbulie, Emeka Emmanuel Oguzie
This review focused on the potential applications of sulfonated carbon–based heterogeneous acid catalysts for the hydrolysis of lignocellulosic biomass (LCB) fuel feedstock and the development of membrane electrode assembly (MEA) for the direct biomass redox flow fuel cell (DBRFFC). LCBs are hydrolysed to yield simple sugars, which are subsequently oxidized over catalysts in the anode tank of the DBRFFC to generate electricity. Ferric chloride used as a catalyst in the DBRFFC is not efficient for glucose production from LCB, such that the power performance of the DBRFFC is affected during glucose oxidation due to low glucose yield from LCB for electron generation. Sulfonated carbon–based solid acid catalysts (SCSACs) have been established as efficient catalysts for the hydrolysis of LCB and as metal catalyst supports for the fabrication of MEA for further oxidation of glucose and its oxidation by‐products. These capabilities of SCSACs can be explored and applied to significantly improve the power output of the DBRFFC through efficient hybrid catalyst design. There is still a scarcity of literature on this subject and their combination with ferric chloride to enhance glucose yield and oxidation in DBRFFC. This gap was filled by discussing the various types of sulfonated carbon–based catalysts, highlighting their synthesis routes, and their applications in organic compound synthesis, and membrane electrode development in DBRFFC. The knowledge derived will certainly be beneficial to researchers willing to improve the performance of DBRFFC through molecular catalyst design and electrode membrane development for application in DBRFFC.
本综述侧重于磺化碳基异构酸催化剂在水解木质纤维素生物质(LCB)燃料原料中的潜在应用,以及直接生物质氧化还原流燃料电池(DBRFFC)膜电极组件(MEA)的开发。低碳生物质经水解后产生单糖,然后在 DBRFFC 阳极槽中的催化剂作用下氧化发电。DBRFFC 中用作催化剂的氯化铁不能有效地从枸橼酸单质中产生葡萄糖,因此在葡萄糖氧化过程中,由于枸橼酸单质中产生电子的葡萄糖产量低,DBRFFC 的发电性能会受到影响。磺化碳基固体酸催化剂(SCSACs)已被确定为用于水解 LCB 的高效催化剂,以及用于制造 MEA 的金属催化剂载体,以进一步氧化葡萄糖及其氧化副产物。我们可以探索并应用 SCSACs 的这些功能,通过高效的混合催化剂设计来显著提高 DBRFFC 的功率输出。关于这一主题以及将 SCSACs 与氯化铁结合以提高 DBRFFC 中的葡萄糖产量和氧化能力的文献仍然很少。通过讨论各种类型的磺化碳基催化剂,重点介绍它们的合成路线,以及它们在有机化合物合成和 DBRFFC 膜电极开发中的应用,填补了这一空白。所获得的知识必将有益于愿意通过分子催化剂设计和电极膜开发来提高 DBRFFC 性能的研究人员。
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引用次数: 0
Enhanced peroxidase‐like activity of MnFe2O4 nanoparticles on halloysite nanotubes for uric acid detection 哈洛来石纳米管上的 MnFe2O4 纳米粒子在检测尿酸时增强的过氧化物酶样活性
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-09-09 DOI: 10.1002/apj.3143
Hengxia Shen, Zhenbo Xiang, Anfang Dang
Nanozymes have significantly advanced sensing assays by replicating native enzyme functions. However, designing nanozymes with high catalytic activity and easy recyclability remains challenging. The study presented here has resulted in the development of a highly efficient and sensitive colorimetric system for the detection of uric acid, utilizing MnFe2O4@HNTs—a novel composite material consisting of MnFe2O4 loaded onto halloysite nanotubes. These nanocomposites exhibited outstanding peroxidase‐like activity and attractive magnetic properties. The catalytic efficiency of the MnFe2O4@HNTs in the oxidation of 3,3′,5,5′‐tetramethylbenzidine, in the presence of H2O2, was remarkable, leading to a distinct color change from colorless to blue. A linear relationship was observed between absorbance and UA concentration in the range of 1–20 μM, with a detection limit as low as 52 nM. Mechanistic investigations revealed that reactive oxygen species (ROS), specifically singlet oxygen (1O2), were generated through the decomposition of H2O2, which is responsible for the peroxidase‐like activity demonstrated by the MnFe2O4@HNTs. The method showed minimal interference from serum substances and high selectivity. Magnetic MnFe2O4 allowed easy separation and maintained over 95% activity after seven reuse cycles. The developed assay was successfully applied to the detection of uric acid in human serum, achieving recoveries greater than 98.60%. This research significantly advances the design of recyclable high‐performance nanozymes and establishes an effective colorimetric sensing platform for UA detection in clinical samples, potentially improving diagnostic tools for healthcare applications.
纳米酶通过复制原生酶的功能,大大推进了传感检测。然而,设计具有高催化活性和易于回收利用的纳米酶仍具有挑战性。本文介绍的研究利用 MnFe2O4@HNT(一种新型复合材料,由负载在哈洛来石纳米管上的 MnFe2O4 组成)开发了一种高效灵敏的比色系统,用于检测尿酸。这些纳米复合材料具有出色的过氧化物酶样活性和诱人的磁性。在 H2O2 的存在下,MnFe2O4@HNTs 在 3,3′,5,5′-四甲基联苯胺的氧化过程中具有显著的催化效率,导致颜色从无色变为蓝色。在 1-20 μM 范围内,吸光度与 UA 浓度呈线性关系,检测限低至 52 nM。机理研究表明,活性氧(ROS),特别是单线态氧(1O2),是通过 H2O2 的分解产生的,这也是 MnFe2O4@HNTs 所显示的过氧化物酶样活性的原因。该方法受血清物质的干扰极小,选择性高。磁性 MnFe2O4 易于分离,在七个重复使用周期后仍能保持 95% 以上的活性。所开发的检测方法被成功应用于人血清中尿酸的检测,回收率超过 98.60%。这项研究极大地推动了可回收高性能纳米酶的设计,并为临床样本中尿酸的检测建立了一个有效的比色传感平台,有望改善医疗应用中的诊断工具。
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引用次数: 0
CO2 capture for environmental remediation with hollow fibre membrane: Impact of air gap and bore fluid ratio onto the morphology and performance 利用中空纤维膜捕获二氧化碳用于环境修复:气隙和孔液比对形态和性能的影响
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-09-05 DOI: 10.1002/apj.3157
Muhd Izzudin Fikry Zainuddin, Abdul Latif Ahmad, Meor Muhammad Hafiz Shah Buddin, Mohamad Alif Adnan
Hollow fibre membrane (HFM) is favourable for carbon dioxide (CO2) due to its high packing density and high volume to area ratio. In this study, the effect of air gap and bore fluid ratio is explored to study its influence on the morphology and separation performance. With high dope extrusion rate (DER), the shear‐induced polymer orientation can be preserved with low air gap which come with the cost of deformed lumen. As such, the coagulant activity of the bore fluid can be reduced by introducing solvent, which in turn reduces rate of phase inversion to prevent sudden contraction of polymer at low air gap, thus allowing proper formation of lumen. With the presence of solvent, the flowability of the dope solution increased due to reduced viscosity as the bore fluid with high solvent content make contact the external coagulant. HFM spun with low air gap with the presence of solvent in the bore fluid shows increased stretched ratio due to the influence of gravitational pull upon being extruded from the spinneret. This in turn improved the polymer chain orientation due to the stretch across the spinning line. Subsequently, HFM spun with 80 wt.% of N‐methyl‐2‐pyrollidone (NMP) in the bore fluid using narrow gap spinneret with 5‐cm air gap shows the highest ideal CO2/N2 and CO2/CH4 selectivity at 23.4 and 28 respectively, even though it also exhibit the lowest CO2 permeance at only 3.1 GPU which was ascribed to the formation of dense skin layer. Meanwhile, when HFM was spun with a bigger annulus gap, the ideal CO2/N2 and CO2/CH4 selectivity slightly dropped, however the CO2 permeance exhibit increment.
中空纤维膜(HFM)因其高堆积密度和高体积面积比而有利于二氧化碳(CO2)的分离。本研究探讨了气隙和孔液比对形态和分离性能的影响。在高涂料挤出率(DER)条件下,剪切力引起的聚合物取向可在低气隙条件下保持,但代价是内腔变形。因此,可以通过引入溶剂来降低孔内流体的凝固活性,进而降低相位反转率,防止聚合物在低气隙时突然收缩,从而使管腔正常形成。由于溶剂含量高的孔液与外部凝固剂接触,粘度降低,从而增加了涂料溶液的流动性。由于从喷丝板挤出时受到重力拉力的影响,在孔液中含有溶剂的情况下,低气隙纺丝的高频熔融材料的拉伸比增加。这反过来又改善了聚合物链在纺丝线上的拉伸取向。随后,使用气隙为 5 厘米的窄间隙喷丝板,在孔液中加入 80 wt.% 的 N-甲基-2-吡咯烷酮(NMP)纺丝的 HFM 显示出最高的理想 CO2/N2 和 CO2/CH4 选择性,分别为 23.4 和 28,尽管它也显示出最低的 CO2 渗透率,仅为 3.1 GPU,这归因于致密表皮层的形成。同时,当 HFM 采用更大的环隙纺丝时,理想的 CO2/N2 和 CO2/CH4 选择性略有下降,但 CO2 渗透率却有所提高。
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引用次数: 0
An insight into the investigation of partition characteristics of flow fields based on chaos fractal theory in a jet impingement–negative‐pressure reactor 基于混沌分形理论的射流冲击-负压反应器中流场分区特征研究的启示
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-09-04 DOI: 10.1002/apj.3155
Yuxi Hu, Yingying Dong, Guangchao Jiang, Zonghan Li, Fachen Qiu
The jet impingement–negative‐pressure reactor (JI‐NPR) is a continuous and efficient technology designed to remove ammonia without clogging. Prior research has discovered that the changing movement of a porous jet impinging under negative‐pressure conditions is distinguished by a more pronounced distribution over many regions. This study utilizes the CFD numerical simulation method in conjunction with the MATLAB platform to investigate the fractal characteristics of water phase distribution, velocity, turbulence intensity, vortex amount, and other parameters at various locations. The fractal dimension is employed as a criterion to analyze the chaotic characteristics of this multi‐area distribution phenomenon. The study demonstrates that the effectiveness of deamination removal can be enhanced by quantitatively assessing the complex characteristics in the fluid flow using the chaotic fractal theory, which facilitates the identification of the ideal parameter settings. The optimal deamination effect can be achieved in the reactor when the jet velocity is set to 3.45 m/s and the negative pressure is maintained at 20 400 Pa.
射流冲击-负压反应器(JI-NPR)是一种连续高效的技术,旨在去除氨气而不会堵塞。先前的研究发现,在负压条件下撞击的多孔射流的运动变化在许多区域的分布更为明显。本研究将 CFD 数值模拟方法与 MATLAB 平台相结合,研究了不同位置的水相分布、速度、湍流强度、漩涡量等参数的分形特征。以分形维数为标准分析了这种多区域分布现象的混沌特征。研究表明,利用混沌分形理论对流体流动中的复杂特性进行定量评估,有助于确定理想的参数设置,从而提高去污效果。当射流速度设定为 3.45 m/s,负压保持在 20 400 Pa 时,反应器中可达到最佳脱氨效果。
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引用次数: 0
Fabrication and performance evaluation of polycarbonate/polyvinyl alcohol–titanium dioxide thin‐film nanocomposite membranes for water treatment 用于水处理的聚碳酸酯/聚乙烯醇-二氧化钛薄膜纳米复合膜的制作和性能评估
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-09-02 DOI: 10.1002/apj.3150
Arian Samiei, Homayun Khezraqa, Habib Etemadi, Elham Shokri
In recent years, there has been growing interest in using polymer nanocomposite membranes as a more advanced method for removing pollutants from water and treating wastewater for various purposes. In this study, thin‐film nanocomposite (TFN) membranes of polycarbonate/polyvinyl alcohol–titanium dioxide thin‐film (PC/PVA–TiO2) were fabricated by dip‐coating a PC substrate in a PVA/TiO2 solution. Various methods, including attenuated total reflectance‐Fourier transform infrared (ATR‐FTIR) spectroscopy, field emission scanning electron microscopy (FE‐SEM), atomic force microscopy (AFM), and water contact angle were utilized to assess the structural characteristics of the produced membranes. The PC/PVA thin‐film composite (TFC) and PC/PVA–TiO2 TFN membranes were then examined in a submerged membrane system to evaluate their effectiveness in filtering humic acid (HA) under various vacuum transmembrane pressure (0.3 and 0.6 bar) condition. The FTIR‐ATR results confirmed the formation of the active layer of PVA/TiO2 nanoparticles (NPs). It was observed that adding 1 wt.% of TiO2 NPs to the active layer of PVA/TiO2 significantly enhanced the water contact angle from 77.5° for PC support to 55.3° for PC/PVA–TiO2 (0.1) TFN membranes. Furthermore, the FE‐SEM results confirmed the formation of an active layer of PVA/TiO2 with a thickness of 237.87 nm. The pure water flux increased from 101.64 L/m2h for the PC/PVA TFC membrane to 144.02 L/m2h and 199.09 L/m2h for the PC/PVA–TiO2 (0.05) and PC/PVA–TiO2 (0.1) TFN membranes, respectively. Also, the results revealed that at lower transmembrane pressure, all membranes showed higher value in HA removal as compared to when higher transmembrane pressure was used.
近年来,人们对使用聚合物纳米复合膜作为去除水中污染物和处理各种用途废水的更先进方法越来越感兴趣。本研究将聚碳酸酯/聚乙烯醇-二氧化钛薄膜(PC/PVA-TiO2)通过在 PVA/TiO2 溶液中浸涂 PC 基质的方法制成了纳米复合薄膜(TFN)。利用各种方法,包括衰减全反射-傅立叶变换红外光谱(ATR-FTIR)、场发射扫描电子显微镜(FE-SEM)、原子力显微镜(AFM)和水接触角来评估所制薄膜的结构特征。然后在浸没膜系统中检测了 PC/PVA 薄膜复合(TFC)和 PC/PVA-TiO2 TFN 膜,以评估它们在不同真空跨膜压力(0.3 和 0.6 巴)条件下过滤腐植酸(HA)的效果。傅立叶变换红外-原子吸收光谱(FTIR-ATR)结果证实了 PVA/TiO2 纳米粒子(NPs)活性层的形成。结果表明,在 PVA/TiO2 活性层中添加 1 wt.% 的 TiO2 NPs 能显著提高水接触角,从 PC 支持层的 77.5°提高到 PC/PVA-TiO2 (0.1) TFN 膜的 55.3°。此外,FE-SEM 结果证实形成了厚度为 237.87 nm 的 PVA/TiO2 活性层。纯水通量从 PC/PVA TFC 膜的 101.64 升/平方米小时分别增加到 PC/PVA-TiO2 (0.05) 和 PC/PVA-TiO2 (0.1) TFN 膜的 144.02 升/平方米小时和 199.09 升/平方米小时。结果还显示,与使用较高跨膜压力时相比,在较低跨膜压力时,所有膜的 HA 去除率都较高。
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引用次数: 0
Numerical investigation of electromagnetic [Cu + TiO2/H2O]h hybrid nanofluid flow with solar radiation over an exponential stretching surface 指数拉伸表面上太阳辐射电磁[Cu + TiO2/H2O]h 混合纳米流体流动的数值研究
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-08-31 DOI: 10.1002/apj.3154
Bhumarapu Venkateswarlu, Sang Woo Joo, Nallagundla Nagendra, Ahmed Sayed M Metwally
The idea of a hybrid nanofluid (HNF) has sparked curiosity among many scientists because of its ability to enhance thermal characteristics, leading to elevated rates of heat transfer (HT). These HNFs are utilized in various engineering and industrial settings, such as electronics cooling, manufacturing, naval structures, biomedical applications, and drug delivery. The current study investigates the analysis of irreversibility in EMHD [Cu + TiO2/H2O]h flow over a stretching sheet with radiation and viscous dissipation. The governing PDEs are converted into ODEs using similarity variables. These ODEs are then solved using the RKF method along with a shooting technique. The effects of different physical parameters on the velocity and temperature distributions of the HNF, as well as on HT and surface drag force, are thoroughly examined and presented in graphs. The velocity of [TiO2/water]n flow declines as the magnetic field strength rises, but it rises with greater electric field values for [Cu + TiO2/water]h. The temperature of the [Cu + TiO2/water]h increases with elevated levels of radiation, Eckert number, and heat generation strength. Higher Reynolds and Brinkman numbers result in a rise in entropy generation for [Cu + TiO2/H2O]h, whereas the Bejan number decreases to the same extent. The HT rate in [Cu + TiO2/H2O]h increases by 3.05% as the Eckert number rises, while it drops by 4.01% when there is significant thermal radiation. Skin friction reduces by 3.21% in [TiO2/water]n as the electric field strength increases, whereas it decreases by 4.05% with an increase in magnetic field strength. These discoveries offer valuable perspectives on furthering the utilization of HNFs in engineering and industrial operations.
混合纳米流体(HNF)的概念引发了许多科学家的好奇,因为它能够增强热特性,从而提高热传导率(HT)。这些 HNF 可用于各种工程和工业领域,如电子冷却、制造、舰船结构、生物医学应用和药物输送。目前的研究调查了 EMHD [Cu + TiO2/H2O]h 在具有辐射和粘性耗散的拉伸片上流动的不可逆性分析。利用相似变量将支配 PDE 转换为 ODE。然后使用 RKF 方法和射击技术对这些 ODEs 进行求解。对不同物理参数对 HNF 的速度和温度分布以及 HT 和表面阻力的影响进行了深入研究,并用图形表示出来。TiO2/water]n 的流速随着磁场强度的增加而降低,但对于 [Cu + TiO2/water]h 而言,随着电场值的增加而升高。Cu + TiO2/水]h的温度随着辐射、埃克特数和发热强度的升高而升高。雷诺数和布林克曼数越高,[Cu + TiO2/H2O]h 的熵产生量越大,而贝扬数的下降幅度相同。随着埃克特数的升高,[Cu + TiO2/H2O]h中的热效率增加了3.05%,而当存在大量热辐射时,热效率下降了4.01%。随着电场强度的增加,[TiO2/水]n 中的皮肤摩擦降低了 3.21%,而随着磁场强度的增加,皮肤摩擦降低了 4.05%。这些发现为在工程和工业操作中进一步利用 HNFs 提供了宝贵的前景。
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引用次数: 0
Preparation and photocatalytic mechanism of magnetic Ag2S/CoFe1.95Dy0.05O4 Z‐scheme heterojunction 磁性 Ag2S/CoFe1.95Dy0.05O4 Z 型异质结的制备与光催化机理
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-08-31 DOI: 10.1002/apj.3153
Liu Qingwang, Xu Mai, Meng Ying
The synthesis of high‐efficiency magnetic composite photocatalyst by doping magnetic cobalt ferrite and compounding single semiconductor photocatalyst is a promising strategy to improve the oxidation ability of photocatalytic systems. In this paper, CoFe1.95Dy0.05O4 (CFDO) was prepared by doping Dy element into magnetic CoFe2O4, and Ag2S (AS)/CFDO with high‐efficiency magnetic photocatalyst was synthesized by compounding AS with CFDO as the substrate. The photocatalytic samples were characterized by different advanced characterization methods, and their photocatalytic degradation of methylene blue (MB) was studied. The results show that AS/CFDO exhibits higher visible light response, excellent photogenerated charge separation ability and migration efficiency, and excellent catalytic performance in the catalytic degradation system. The photocatalytic activity of AS/CFDO was the highest, and its photocatalytic degradation kinetic constant K was 2.48 and 1.54 times that of AS and CFDO, respectively. In addition, the catalyst contained in the catalytically contaminated solution can be effectively separated by an external magnetic field to achieve multiple cycles of degradation and recycling. The cyclic degradation experiments showed that AS/CFDO exhibited high degradation stability during the photodegradation process. After the fifth reuse, the degradation efficiency was still more than 88.0%. Finally, the possible photocatalytic mechanism of the samples was discussed. Therefore, this work provides an effective solution for the construction of photocatalysts with high efficiency, magnetic recovery, and cyclic degradation stability and avoids the secondary pollution of catalysts to organic wastewater. It is of great significance to create an environmentally friendly catalytic method for efficient cyclic degradation of organic wastewater.
通过掺杂磁性钴铁氧体和复合单一半导体光催化剂来合成高效磁性复合光催化剂,是提高光催化体系氧化能力的一种很有前途的策略。本文通过在磁性 CoFe2O4 中掺杂镝元素制备了 CoFe1.95Dy0.05O4(CFDO),并以 CFDO 为基底与 AS 复合合成了 Ag2S(AS)/CFDO 高效磁性光催化剂。采用不同的先进表征方法对光催化样品进行了表征,并研究了它们对亚甲基蓝(MB)的光催化降解作用。结果表明,AS/CFDO 在催化降解体系中表现出更高的可见光响应、优异的光生电荷分离能力和迁移效率以及优良的催化性能。AS/CFDO 的光催化活性最高,其光催化降解动力学常数 K 分别是 AS 和 CFDO 的 2.48 倍和 1.54 倍。此外,催化污染溶液中所含的催化剂可通过外加磁场有效分离,实现多次循环降解和回收利用。循环降解实验表明,AS/CFDO 在光降解过程中表现出较高的降解稳定性。第五次重复使用后,降解效率仍超过 88.0%。最后,讨论了样品可能的光催化机理。因此,这项工作为构建具有高效率、磁性恢复和循环降解稳定性的光催化剂提供了有效的解决方案,并避免了催化剂对有机废水的二次污染。这对于创造一种高效循环降解有机废水的环境友好型催化方法具有重要意义。
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引用次数: 0
Physicochemical influence of graphite agent for fabrication of MoVTeNbO catalyst for direct oxidation of propene to acrylic acid 石墨剂对制造用于丙烯直接氧化成丙烯酸的 MoVTeNbO 催化剂的物理化学影响
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-08-30 DOI: 10.1002/apj.3149
Hossein Khosravi Rouzbahani, Azam Akbari, Golshan Mazloom
MoV‐based composites stand out as the most promising potential catalysts targeted for direct production of acrylic acid from alkane/alkene substances. Herein, MoVTeNbO powder was synthesized and successfully fabricated by adding graphite as an appropriate tableting agent. Without employing graphite as lubricant, the fabrication of tablets was not practicable. The physicochemical effects of graphite on the catalyst properties were investigated via characterization by X‐ray diffraction (XRD), Brunauer–Emmett–Teller (BET), scanning electron microscopy (SEM), ammonia temperature‐programmed desorption (NH3‐TPD), and thermal gravimetric analysis (TGA) methods. In addition to the easy and operative formation of tablets by consisting graphite, TGA results indicated better thermal stability compared to the bare powder. No harmful impact of graphite on the catalyst crystalline phases and morphology was detected by XRD and SEM analysis. The SEM images proved the graphite incorporation as a binder in the physical combination of the catalyst particles along the compression process, resulting in the desired physical resistance. Graphite caused a slight decrease in the BET surface area and final catalyst acidity. Despite the effect of reducing propene conversion, interestingly, a substantial improvement in the yield of acrylic acid was found by tableting. The graphite as an inert agent suppressed hot spots on the catalyst surface, leading to superior consistency in activity over time as well as lower selectivity to undesirable COx.
MoV 基复合材料是最有前途的潜在催化剂,可用于从烷烃/烯烃物质直接生产丙烯酸。本文合成了 MoVTeNbO 粉末,并通过添加石墨作为适当的压片剂成功制成。如果不使用石墨作为润滑剂,则无法制作片剂。通过 X 射线衍射 (XRD)、Brunauer-Emmett-Teller (BET)、扫描电子显微镜 (SEM)、氨温程控解吸 (NH3-TPD) 和热重分析 (TGA) 等方法研究了石墨对催化剂性能的物理化学影响。与裸粉末相比,TGA 结果表明,石墨不仅易于形成片剂,而且操作简便。通过 XRD 和 SEM 分析,没有发现石墨对催化剂晶相和形态造成有害影响。扫描电子显微镜图像证明,在压缩过程中,石墨是催化剂颗粒物理结合的粘合剂,从而产生了理想的物理阻力。石墨导致 BET 表面积和最终催化剂酸度略有下降。尽管会降低丙烯的转化率,但有趣的是,通过压片,丙烯酸的产率得到了大幅提高。石墨作为一种惰性剂,抑制了催化剂表面的热点,从而使催化剂的活性长期保持优异的一致性,并降低了对不良 COx 的选择性。
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引用次数: 0
Experimental studies on mechanism whereby premixed chamber length and equivalence ratio collaboratively influence self‐excited thermoacoustic instability 预混室长度和等效比共同影响自激热声不稳定性机理的实验研究
IF 1.8 4区 工程技术 Q3 Chemical Engineering Pub Date : 2024-08-28 DOI: 10.1002/apj.3145
Yuanhang Zhang, Yongbo Du, Jingkun Zhang, Defu Che
Self‐excited thermoacoustic instability (SETAI) is a dangerous phenomenon in combustion equipment. While it is widely acknowledged that SETAI behavior is determined by the couple between pressure and heat release oscillation, their phase difference is difficult to predict, which impedes the development of SETAI control technology. With the aim of passive control technology development, this paper conducted experiment on a premixed hedge combustor to explore the mechanism whereby premixed chamber length (LP) and equivalence ratio (φ) collaboratively influence SETAI behavior. Results showed LP mainly affects the pressure mode shape within premixed chamber and consequently alters the phase difference between pressure and flowrate oscillation at combustion chamber inlet. Changing φ gives rise to different reaction time‐lag (τ), thus altering the phase difference between flowrate and reaction heat release oscillation. By introducing this flowrate oscillation, how LP and φ collaboratively determine phase difference between pressure oscillation and heat release oscillation was clarified. The mechanisms identified in this study are consistent with the emerging rationalization of the factors contributing to SETAI, and also provides better understanding on Rayleigh criterion and guidance for SETAI control. With further work on heat release and flow rate measurement, as well as the development on τ description, SETAI can be better predicted and controlled.
自激热声不稳定性(SETAI)是燃烧设备中的一种危险现象。虽然人们普遍认为 SETAI 行为是由压力振荡和放热振荡之间的耦合决定的,但它们之间的相位差很难预测,这阻碍了 SETAI 控制技术的发展。为了开发被动控制技术,本文在预混对冲燃烧器上进行了实验,探索预混室长度(LP)和等效比(φ)共同影响 SETAI 行为的机理。结果表明,LP 主要影响预混室内的压力模式形状,从而改变燃烧室入口处压力和流量振荡之间的相位差。改变φ会产生不同的反应时滞(τ),从而改变流量和反应放热振荡之间的相位差。通过引入这种流速振荡,阐明了 LP 和 φ 如何共同决定压力振荡和放热振荡之间的相位差。本研究确定的机理与正在形成的导致 SETAI 的合理因素相一致,同时也为雷利准则提供了更好的理解,并为 SETAI 控制提供了指导。随着热释放和流速测量工作的进一步开展,以及 τ 描述的发展,SETAI 可以得到更好的预测和控制。
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Asia-Pacific Journal of Chemical Engineering
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