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Exploring semisolid liquid metal anode for lithium-ion battery 探索用于锂离子电池的半固态液态金属阳极
Pub Date : 2024-10-30 DOI: 10.1016/j.nxener.2024.100206
Pisong Cui , Huimin Liu , Xunyong Jiang
Due to their high surface tension and mobility, liquid metals present a challenge for direct coating onto current collectors. Herein, the researchers prepared a semisolid liquid metal by mixing GaInSn liquid metal with copper particle fillers. This semisolid liquid metal's viscosity is suitable for coating and strongly bonding with the current collector without a binder. Though promising, the lithium storage performance of such semisolid liquid metals has remained largely unexplored. The electrodes displayed favorable electrical conductivity and a high initial discharge capacity of 214 mAh g−1. Their discharge process involved a self-healing mechanism through the liquid-state transformation of the active component, analogous to metallic liquid systems. This work overcame the persistent liquid metal coating difficulty by modulating viscosity while revealing their notable lithium storage capabilities.
由于液态金属具有较高的表面张力和流动性,在集电极上直接镀膜是一项挑战。为此,研究人员将 GaInSn 液态金属与铜颗粒填料混合,制备出一种半固态液态金属。这种半固态液态金属的粘度适合涂覆,并能在不使用粘合剂的情况下与电流收集器牢固结合。虽然这种半固态液态金属的储锂性能前景广阔,但在很大程度上仍未得到开发。这些电极显示出良好的导电性和高达 214 mAh g-1 的初始放电容量。它们的放电过程涉及一种通过活性成分的液态转化进行自我修复的机制,类似于金属液态系统。这项研究通过调节粘度克服了长期存在的液态金属涂层难题,同时揭示了其显著的锂存储能力。
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引用次数: 0
Integrating manganese oxide nanoparticles with functionalized carbon nanotubes on carbon cloth to serve as a stable anode for high-capacity Li-ion cells 在碳布上整合氧化锰纳米粒子和功能化碳纳米管,作为高容量锂离子电池的稳定阳极
Pub Date : 2024-10-26 DOI: 10.1016/j.nxener.2024.100207
Merin K. Wilson , Dhanya P. Jacob , Aldrin Antony , M.K. Jayaraj , S. Jayalekshmi
Globally, energy demands are massive, and environmental issues are rising against our sustainability. To maximize the use of renewable energy sources, development of efficient energy storage systems is mandatory. Lithium-ion batteries (LIBs) play an indispensable role in powering portable devices and electric vehicles, due to their high specific capacity and long cycle life. Manganese oxide (Mn3O4) is an environmentally friendly anode active material with high theoretical specific capacity of 936 mAh g−1 for applications in Li-ion cells.
In the present work, Mn3O4-functionalized carbon nanotubes (FCNT) nanocomposite, coated on carbon cloth (CC) current collector and termed as Mn3O4-FCNT @CC, is used as the anode material. Li-ion coin cells based on this nanocomposite anode show discharge capacity of 1371 mAh g−1 and charge capacity of 1141 mAh g−1 at current density of 100 mA g−1 with initial Coulombic efficiency of 83%. After 70 cycles, the charge-discharge capacities of the cells are 953 mAh g−1 and 958 mAh g−1, respectively, with capacity retention of 91% at current rate of 100 mA g−1. These cells are found to deliver reversible charge capacity of 575 mAh g−1 after 100 cycles at 1C (∼1 A g−1) and offer prospects of stable operation at high current rates.
在全球范围内,能源需求巨大,环境问题也日益严重,不利于我们的可持续发展。为了最大限度地利用可再生能源,必须开发高效的储能系统。锂离子电池(LIB)具有比容量大、循环寿命长的特点,在为便携式设备和电动汽车供电方面发挥着不可或缺的作用。氧化锰(Mn3O4)是一种环境友好型阳极活性材料,理论比容量高达 936 mAh g-1,可应用于锂离子电池。在电流密度为 100 mA g-1 时,基于这种纳米复合阳极的锂离子纽扣电池的放电容量为 1371 mAh g-1,充电容量为 1141 mAh g-1,初始库仑效率为 83%。经过 70 次循环后,电池的充放电容量分别为 953 mAh g-1 和 958 mAh g-1,在 100 mA g-1 的电流密度下,容量保持率为 91%。这些电池在 1C 条件下循环 100 次后,可提供 575 mAh g-1 的可逆充电容量(∼1 A g-1),并有望在高电流速率下稳定运行。
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引用次数: 0
Energy storage technology and its impact in electric vehicle: Current progress and future outlook 储能技术及其对电动汽车的影响:当前进展与未来展望
Pub Date : 2024-10-25 DOI: 10.1016/j.nxener.2024.100202
Mohammad Waseem , G. Sree Lakshmi , Mumtaz Ahmad , Mohd Suhaib
The desirable characteristics of an energy storage system (ESS) to fulfill the energy requirement in electric vehicles (EVs) are high specific energy, significant storage capacity, longer life cycles, high operating efficiency, and low cost. In order to advance electric transportation, it is important to identify the significant characteristics, pros and cons, new scientific developments, potential barriers, and imminent prospects of various energy storage technology. The objective of current research is to analyse and find out the optimal storage technology among different electro-chemical, chemical, electrical, mechanical, and hybrid storage system. Different batteries including lead-acid, nickel-based, lithium-ion, flow, metal-air, solid state, and ZEBRA along with their operating parameters are reviewed. The potential roles of fuel cell, ultracapacitor, flywheel and hybrid storage system technology in EVs are explored. Performance parameters of various battery system are analysed through radar based specified technique to conclude the best storage medium in electric mobility. Additionally, the current study compiles a critical analysis of 264 publications from various sources.
为满足电动汽车(EV)的能源需求,储能系统(ESS)应具备以下理想特性:比能量高、存储容量大、生命周期长、运行效率高和成本低。为了推动电动交通的发展,必须明确各种储能技术的显著特点、利弊、新的科学发展、潜在障碍和即将到来的前景。当前研究的目标是分析和找出不同电化学、化学、电气、机械和混合存储系统中的最佳存储技术。研究回顾了不同的电池,包括铅酸电池、镍基电池、锂离子电池、液流电池、金属-空气电池、固态电池和 ZEBRA 电池及其运行参数。探讨了燃料电池、超级电容器、飞轮和混合存储系统技术在电动汽车中的潜在作用。通过基于雷达的特定技术分析了各种电池系统的性能参数,从而得出电动汽车中最佳存储介质的结论。此外,本研究还对 264 篇不同来源的出版物进行了批判性分析。
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引用次数: 0
Enhanced photocatalytic performance of hydrothermally synthesized TiO2 nanowires for H2 production via water splitting 增强水热合成 TiO2 纳米线的光催化性能,通过水分离产生 H2
Pub Date : 2024-10-25 DOI: 10.1016/j.nxener.2024.100205
Niteen Jawale, Govind Umarji, Shubhangi Damkale, Sudhir Arbuj
The effective separation and high mobility of photogenerated charge carriers are important in order to enhance the photocatalytic activity of material. The one-dimensional nanostructures are providing the path for the photogenerated charge carriers resulting higher photocatalytic activity. Herein, highly crystalline Titanium dioxide (TiO2) nanowires (TNWs) having anatase phase were synthesized using hydrothermal method by varying the reaction time and temperatures. The synthesized TNWs were characterized using various techniques. Structural study revealed the formation of anatase TiO2 along with a minor percentage of the rutile phase. Morphological study indicates the growth of TiO2 nanowires originated from spheres-wires-flakes as a function of reaction time and temperature. FE-TEM image of TiO2 nanowires prepared at 150 ℃ for 72 h shows complete formation of nano-wires with 7–10 nm diameter. Photocatalytic performance of the synthesized TiO2 nanowires was investigated by observing the hydrogen (H2) generation via water splitting and degradation of aqueous methylene blue (MB) dye under a 400 W mercury vapor lamp respectively. Among the prepared samples, the TiO2 nanowires prepared at 150 ℃ for 48 h showed the highest H2 generation of 7464.28 μmol/0.1 gm higher than the Degussa TiO2. Further, the same nanostructured TiO2 shows the 100% MB degradation within 30 min (Kapp = 13.54 × 10−2 min−1).
光生电荷载流子的有效分离和高迁移率对于提高材料的光催化活性非常重要。一维纳米结构为光生电荷载流子提供了路径,从而提高了光催化活性。本文采用水热法,通过改变反应时间和温度,合成了具有锐钛矿相的高结晶二氧化钛(TiO2)纳米线(TNWs)。利用各种技术对合成的 TNWs 进行了表征。结构研究表明形成了锐钛型二氧化钛和少量金红石相。形态学研究表明,随着反应时间和温度的变化,TiO2 纳米线从球状-线状-片状生长。在 150 ℃ 下制备 72 h 的 TiO2 纳米线的 FE-TEM 图像显示,直径为 7-10 nm 的纳米线已完全形成。在 400 W 汞蒸汽灯下,分别观察了通过水分裂产生氢气(H2)和降解亚甲基蓝(MB)染料的情况,从而研究了合成的 TiO2 纳米线的光催化性能。在制备的样品中,在 150 ℃ 下制备 48 小时的 TiO2 纳米线的氢气生成量最高,比 Degussa TiO2 高 7464.28 μmol/0.1gm。此外,同样的纳米结构二氧化钛在 30 分钟内显示出 100% 的甲基溴降解率(Kapp = 13.54 × 10-2 min-1)。
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引用次数: 0
Facile synthesis of K0.5Mn2O4·1.5H2O/rGO composites with ultrahigh zinc storage properties 轻松合成具有超高储锌性能的 K0.5Mn2O4-1.5H2O/rGO 复合材料
Pub Date : 2024-10-24 DOI: 10.1016/j.nxener.2024.100204
Shuo Li , Shan Wang , Yanxuan Chen , Xianliang Meng , Lin Wang , Junsheng Zhu
Zinc-ion batteries have drawn much attention due to their good safety and low cost. In this work, a straightforward 1-pot pyrolysis process has been utilized to prepare novel K0.5Mn2O4·1.5H2O/rGO (KMrGO) composites. In KMrGO, the layered structure of reduced graphene oxide (rGO) can efficiently improve the electrical conductivity of K0.5Mn2O4·1.5H2O, enabling KMrGO to demonstrate high zinc storage performance. Although a very small amount of rGO (∼1.8%) has been introduced, the reversible capacity of KMrGO reaches 230.1 mAh g−1 after 250 cycles at 0.2 A g−1. Even after 1200 cycles at a high current density of 1 A g−1, KMrGO remains a good capacity retention of 70.2%. Considering the simple preparation of KMrGO, this method can provide a new route for synthesizing other metal dioxide/rGO composites.
锌离子电池因其良好的安全性和低成本而备受关注。在这项研究中,我们利用简单的单锅热解工艺制备了新型 K0.5Mn2O4-1.5H2O/rGO (KMrGO) 复合材料。在 KMrGO 中,还原氧化石墨烯(rGO)的层状结构可有效改善 K0.5Mn2O4-1.5H2O 的导电性,从而使 KMrGO 具有较高的锌储存性能。虽然引入了极少量的 rGO(∼1.8%),但在 0.2 A g-1 的条件下循环 250 次后,KMrGO 的可逆容量达到了 230.1 mAh g-1。即使在 1 A g-1 的高电流密度下循环 1200 次,KMrGO 的容量保持率仍高达 70.2%。考虑到 KMrGO 的简单制备,该方法为合成其他金属二氧化物/rGO 复合材料提供了一条新途径。
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引用次数: 0
A systematic investigation on the hybrid Darrieus-Savonius vertical axis wind turbine aerodynamic performance and self-starting capability improvement by installing a curtain 通过安装帘幕改善达里厄斯-萨沃纽斯混合垂直轴风力涡轮机气动性能和自启动能力的系统研究
Pub Date : 2024-10-24 DOI: 10.1016/j.nxener.2024.100203
Farzad Ghafoorian , Seyed Reza Mirmotahari , Mohammad Eydizadeh , Mehdi Mehrpooya
The Darrieus vertical axis wind turbine is categorized as a lift-based power generation turbomachine. However, the challenge of self-starting capability poses a potential obstacle for this turbine. This study addressed this issue by incorporating a Savonius rotor and introducing a Darrieus-Savonius hybrid rotor to enhance the aerodynamic performance and self-starting capability. The results demonstrated a substantial increase in power coefficient by 64% at tip speed ratio (TSR) = 1.4. Furthermore, the curtain installation was investigated as a mechanism to improve rotor performance. The findings indicated that the multiplication of a curtain enhanced the self-starting capability by controlling the positive pressure gradient on the suction and pressure sides of the rotor blades. Notably, considering the flow physics and rotor efficiency in the presence of the curtain with walls featuring different angles, it was established that the optimal angles for the upper and lower walls are 20° and 45°, respectively. This configuration led to a 35% increase in rotor efficiency compared to the solo hybrid rotor. The hybrid rotor demonstrated superior performance within the low-TSR range values, while the Darrieus control case exhibited better efficiency in the high-TSR range. Despite the enhancement in performance attributed to the curtain installation, the high-TSR range still lagged behind the Darrieus control case.
达里厄斯垂直轴风力涡轮机属于升力发电涡轮机。然而,自启动能力的挑战对这种涡轮机构成了潜在的障碍。为解决这一问题,本研究采用了萨沃尼乌斯转子,并引入了达里厄斯-萨沃尼乌斯混合转子,以提高气动性能和自启动能力。结果表明,在叶尖速度比 (TSR) = 1.4 时,功率系数大幅提高了 64%。此外,还研究了帘幕安装作为提高转子性能的机制。研究结果表明,通过控制转子叶片吸入侧和压力侧的正压力梯度,帘幕的增殖增强了自启动能力。值得注意的是,考虑到帘幕存在时的流动物理和转子效率,帘幕壁具有不同的角度,确定上下壁的最佳角度分别为 20° 和 45°。与单独的混合转子相比,这种配置使转子效率提高了 35%。混合式转子在低 TSR 值范围内表现出卓越的性能,而达里厄斯控制案例在高 TSR 值范围内表现出更高的效率。尽管帘式安装提高了性能,但高 TSR 范围仍然落后于达里厄斯控制情况。
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引用次数: 0
Indented metallic bipolar plates for vanadium redox flow batteries 用于钒氧化还原液流电池的凹陷金属双极板
Pub Date : 2024-10-21 DOI: 10.1016/j.nxener.2024.100201
Laxman Kumar Kundarapu , M. Maruthi Prasanna , Sreenivas Jayanti
The standard industrial vanadium redox flow battery (VRFB) stack is made of thick graphite bipolar plates to support the flow field required for optimal circulation of electrolyte. These thick plates suffer from electrolyte seepage, poor mechanical properties, and high machining and processing costs. In the present study, we report on the use of metallic bipolar plates for the construction of the VRFB cell. We show, through comprehensive electrochemical and hydrodynamic investigations, that Hastelloy C276, a corrosion-resistant high Nickel alloy, is a suitable bipolar plate material in VRFB cells. We show further that surface texture modification, in the form of a mix of concave and convex spherical indentations on the metallic bipolar plate, can have beneficial effects on cell performance. Comparative experiments on medium-size cells of a nominal area of 440 cm2 operating in the current density range of 75–125 mA/cm2 show that discharge energy gains of 25% or higher can be obtained together with a 10–15% reduction in pressure drop in comparison with similar cells with flat bipolar plates. It is posited that the concave indentations spread over the entire area ensure uniform electrolyte circulation while regions of low and high electrode compression create flow channeling possibilities that lead to reduced pressure drop.
标准的工业钒氧化还原液流电池(VRFB)堆栈由厚石墨双极板制成,以支持电解液最佳循环所需的流场。这些厚板存在电解液渗漏、机械性能差以及加工和处理成本高等问题。在本研究中,我们报告了使用金属双极板建造 VRFB 电池的情况。通过全面的电化学和流体力学研究,我们发现哈氏合金 C276(一种耐腐蚀的高镍合金)是一种适用于 VRFB 电池的双极板材料。我们进一步证明,在金属双极板上以凹凸球形压痕混合的形式进行表面纹理修饰,可对电池性能产生有利影响。对标称面积为 440 cm2 的中型电池进行的比较实验表明,与采用平面双极板的类似电池相比,在电流密度为 75-125 mA/cm2 的范围内工作时,放电能量可提高 25% 或更高,压降也可降低 10-15%。据推测,遍布整个区域的凹陷压痕确保了电解液的均匀循环,而低电极压缩区域和高电极压缩区域则创造了导流的可能性,从而降低了压降。
{"title":"Indented metallic bipolar plates for vanadium redox flow batteries","authors":"Laxman Kumar Kundarapu ,&nbsp;M. Maruthi Prasanna ,&nbsp;Sreenivas Jayanti","doi":"10.1016/j.nxener.2024.100201","DOIUrl":"10.1016/j.nxener.2024.100201","url":null,"abstract":"<div><div>The standard industrial vanadium redox flow battery (VRFB) stack is made of thick graphite bipolar plates to support the flow field required for optimal circulation of electrolyte. These thick plates suffer from electrolyte seepage, poor mechanical properties, and high machining and processing costs. In the present study, we report on the use of metallic bipolar plates for the construction of the VRFB cell. We show, through comprehensive electrochemical and hydrodynamic investigations, that Hastelloy C276, a corrosion-resistant high Nickel alloy, is a suitable bipolar plate material in VRFB cells. We show further that surface texture modification, in the form of a mix of concave and convex spherical indentations on the metallic bipolar plate, can have beneficial effects on cell performance. Comparative experiments on medium-size cells of a nominal area of 440 cm<sup>2</sup> operating in the current density range of 75–125 mA/cm<sup>2</sup> show that discharge energy gains of 25% or higher can be obtained together with a 10–15% reduction in pressure drop in comparison with similar cells with flat bipolar plates. It is posited that the concave indentations spread over the entire area ensure uniform electrolyte circulation while regions of low and high electrode compression create flow channeling possibilities that lead to reduced pressure drop.</div></div>","PeriodicalId":100957,"journal":{"name":"Next Energy","volume":"6 ","pages":"Article 100201"},"PeriodicalIF":0.0,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142535859","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dry reforming of methane and interaction between NiO and CeZrPrOx oxide in different crystallographic plane 甲烷的干重整以及不同晶面的氧化镍和氧化 CeZrPrOx 之间的相互作用
Pub Date : 2024-10-17 DOI: 10.1016/j.nxener.2024.100199
Amir Hassan , Yaroslavl Utkin
Methane dry reforming (DRM) holds promise as a pathway for converting methane into valuable synthesis gas (syngas) and high-value chemicals. In this study, we investigate the crystallographic plane interactions between nickel oxide (NiO) and a modified ceria-zirconia-praseodymium oxide support (CeZrPrOx) to elucidate their influence on catalytic activity in methane dry reforming. X-ray diffraction (XRD) patterns and transmission electron microscopy (TEM) techniques were employed to characterize the catalyst. Our findings reveal that specific crystallographic planes significantly impact the catalytic performance of NiO/CeZrPrOx catalyst. The (111), (110), and (100) facets of the support material are examined for their interactions with NiO. We observe that the (110) plane of the support exhibits strong interaction with NiO, leading to enhanced catalytic activity. This interaction facilitates superior anchoring of Ni nanoparticles, lowering sintering and promoting a strong metal-support interaction effect (SMSI). Additionally, our analysis suggests that the (110) interface is particularly favorable for methane dry reforming. Overall, this study highlights the importance of crystallographic plane interactions in NiO/CeZrPrOx catalysts and offers valuable insights for optimizing catalyst design for methane conversion processes.
甲烷干重整(DRM)有望成为将甲烷转化为有价值的合成气(Syngas)和高价值化学品的途径。在本研究中,我们研究了氧化镍(NiO)与改性铈-氧化锆-氧化镨支撑物(CeZrPrOx)之间的晶面相互作用,以阐明它们对甲烷干重整催化活性的影响。我们采用 X 射线衍射 (XRD) 图谱和透射电子显微镜 (TEM) 技术对催化剂进行了表征。我们的研究结果表明,特定的晶面会对 NiO/CeZrPrOx 催化剂的催化性能产生重大影响。我们研究了支撑材料的 (111)、(110) 和 (100) 面与 NiO 的相互作用。我们观察到,支撑材料的 (110) 面与氧化镍有很强的相互作用,从而提高了催化活性。这种相互作用促进了镍纳米颗粒的良好锚定,降低了烧结,并促进了强烈的金属-支撑相互作用效应(SMSI)。此外,我们的分析表明,(110) 界面特别有利于甲烷干重整。总之,这项研究强调了结晶平面相互作用在 NiO/CeZrPrOx 催化剂中的重要性,并为优化甲烷转化工艺的催化剂设计提供了宝贵的见解。
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引用次数: 0
Hierarchical control of inverter-based microgrid with droop approach and proportional-integral controller 采用下垂方法和比例积分控制器对基于逆变器的微电网进行分级控制
Pub Date : 2024-10-14 DOI: 10.1016/j.nxener.2024.100200
Mahmoud Hazhir
By increasing the penetration of renewable resources in power systems, which are mostly inverter-based, voltage and frequency control has faced many challenges. Unlike the synchronous generators in large power systems, these sources have no resistance against load changes due to their low inertia, therefore, controlling the voltage and frequency of inverter-based microgrids requires new approaches. In this article, by taking feedback from the output voltage and current of the inverter and using the Proportional Integral controller, the desired control signal to be applied to the inverter is obtained in a way that initially creates a phase and voltage difference between the DGs in the microgrid, the power flow is established in a way that without the need for any communication link, the balance of energy production and consumption is established in an island mode, and at the end, the voltage and frequency of Distributed Generations are restored to their nominal values. The presented control logic is also implemented in Simulink MATLAB software and its results are measured and evaluated.
随着可再生能源在电力系统中的渗透率不断提高,电压和频率控制面临着许多挑战。与大型电力系统中的同步发电机不同,这些资源由于惯性小,对负载变化没有阻力,因此,控制基于逆变器的微电网的电压和频率需要新的方法。在本文中,通过从逆变器的输出电压和电流中获取反馈信息,并使用比例积分控制器,可以获得应用于逆变器的所需控制信号,从而在微电网中的分布式发电机之间产生相位差和电压差,在不需要任何通信链路的情况下建立电力流,在孤岛模式下建立能源生产和消费的平衡,最后将分布式发电机的电压和频率恢复到额定值。提出的控制逻辑也在 Simulink MATLAB 软件中实现,并对其结果进行了测量和评估。
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引用次数: 0
Assessment of Iron(III) chloride as a catalyst for the production of hydrogen from the supercritical water gasification of microalgae 评估氯化铁(III)作为微藻超临界水气化制氢催化剂的效果
Pub Date : 2024-10-10 DOI: 10.1016/j.nxener.2024.100198
Kieran Heeley , Rafael L. Orozco , Imogen Sheppard , Lynne E. Macaskie , John Love , Bushra Al-Duri
Alkali metal salts and supported transition metals have been the dominant catalysts used to maximise hydrogen production from supercritical water gasification (SCWG). Recently, FeCl3 has emerged as an alternative to these that has been found to be more effective in some cases reported in literature. However, to these authors’ knowledge, few studies exist that study this catalyst with none that involve microalgae as the feedstock. Investigation is reported into the effect of FeCl3 on the SCWG of Chlorella vulgaris for a range of temperatures (400–600 °C) and biomass concentrations (1–3 wt%), with comparisons made to other catalysts (KOH, Ru/C and their combinations). A significant decrease in hydrogen yield, carbon conversion and energy efficiency was observed with the addition of FeCl3, due to a reduced pH which suppressed the water gas shift reaction and catalysed of char forming reactions. This was in contrary to Ru/C and KOH catalysts, where those outcomes increased. Additionally, when FeCl3 was used with Ru/C, the ruthenium was poisoned, nullifying its positive effects. Consequently, FeCl3 is not a suitable catalyst for hydrogen production from microalgae, either alone or in conjunction with a ruthenium catalyst.
碱金属盐和支撑过渡金属一直是用于最大化超临界水气化(SCWG)制氢的主要催化剂。最近,FeCl3 作为这些催化剂的替代品出现了,在文献报道的一些案例中发现它更为有效。然而,据作者所知,对这种催化剂的研究很少,而且没有一项研究涉及微藻作为原料。报告调查了 FeCl3 在一定温度(400-600 °C)和生物质浓度(1-3 wt%)范围内对小球藻 SCWG 的影响,并与其他催化剂(KOH、Ru/C 及其组合)进行了比较。加入 FeCl3 后,由于 pH 值降低,抑制了水气变换反应并催化了成炭反应,氢气产量、碳转化率和能效都明显降低。这与 Ru/C 和 KOH 催化剂相反,在这两种催化剂中,这些结果都有所增加。此外,当氯化铁与 Ru/C 一起使用时,钌会中毒,从而抵消了其积极作用。因此,无论是单独使用氯化铁还是与钌催化剂一起使用,氯化铁都不适合作为微藻制氢的催化剂。
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引用次数: 0
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