检索结果-内蒙古大学图书馆

SSRN 2024年

作者： Huang, Heng Zhou, Zhifu Wu, Wei-Tao Wei, Lei Lyu, Jizu Hu, Chengzhi Gao, Linsong Li, Yubai Song, Yongchen Key Laboratory of Ocean Energy Utilization and Energy Conservation of Ministry of Education Dalian University of Technology Dalian116023 China State Key Laboratory of Multiphase Flow in Power Engineering Xi'an Jiaotong University Xi'An710049 China School of Mechanical Engineering Nanjing University of Science and Technology Nanjing210094 China Department of Mechanical and Energy Engineering Southern University of Science and Technology Shenzhen518055 China School of Mechanical Engineering Guangdong Ocean University Zhanjiang524088 China School of Mechanical Engineering and Mechanics Xiangtan University Xiangtan411105 China

The structure and spatial distribution of electrochemical inert phase (EIP) in electrodes are highly heterogeneous, which deteriorates the performance of electrodes under harsh operating conditions such as high-rate or low-temperature. In this work, with the assist of digitally processed X-ray computed tomography (XCT) for charactering images of LiNi0.5Co0.2Mn0.3 electrode, the electrodes with different EIP geometries are reconstructed, and the dependence of electrode performance degradation on EIP is elucidated from a multiscale perspective. Physical structure characterization and 3D microstructure resolved model reveal that, compared to 3D bulk EIP (B-EIP), 2D film EIP (F-EIP) tends to cover active surface of active material (AM), which exacerbates the heterogeneous electrode lithiation reaction. The decrease of AM active surface area makes the state of lithiation (SOL) of particles closely related to their active specific surface area (αa). The temperature sensitivity of electrodes at low temperatures exacerbates the hazard of αa loss, allowing heterogeneous reaction transfer between particles. The Biot number (Bi) evaluates the competing mechanisms between interfacial reactions and bulk diffusion of particles, and the reaction rate at the particle/electrolyte interface is accelerated in high content EIP electrodes, allowing the Li concentration gradient within the particles to be dominated by interfacial reactions. Finally, the electrochemistry and heat generation from particle to electrode level in high area-loaded electrodes are explored, showing that the lithium ion diffusion in the pores controls the interfacial reactions and heat transport behavior. The aggregated high flux reactions and localized hot spots aggravate the heterogeneous degradation and side reactions of the electrode. © 2024, The Authors. All rights reserved.

关键词： Lithium-ion batteries

来源：评论

学校读者我要写书评

暂无评论

Insight into the key Role of Imine Groups in Polyaniline for Adsorbing Heavy Metal Ions: Density Functional Theory and Experimental Study

SSRN

引用

SSRN 2023年

作者： Shi, Bofang Li, Hang Fu, Xiaojie Zhao, Chengcheng Wang, Angelina H. Tan, Weilin Rao, Yongfang Li, Mingtao Komarneni, Sridhar Yang, Honghui Xi’an Key Laboratory of Sustainable Energy Materials Chemistry Department of Applied Chemistry School of Chemistry Xi’an Jiaotong University Xi’an710049 China State Key Laboratory of Multiphase Flow in Power Engineering Department of Environmental Science and Engineering School of Energy and Power Engineering Xi’an Jiaotong University Xi’an710049 China Department of Ecosystem Science and Management Materials Research Institute 204EEL The Pennsylvania State University University ParkPA16802 United States

In polyaniline (PANI) or PANI-based adsorbents, views on which nitrogen group has the highest chemical affinity to heavy metal ions and dominates the adsorption process remain in debate. Herein, we focus on deciphering the main adsorption sites and adsorption mechanisms of PANI using both density functional theory (DFT) calculations and experiments. The theoretical DFT calculations reveal that −N= group, rather than other groups within PANI, is the adsorption site. And the key step of PANI adsorption process is a ligand exchange reaction. In addition, H+ ions with a higher affinity to −N= group can inhibit the adsorption of metal ions through the consumption of adsorption sites and ion exchange reaction. X-ray photoelectron spectra (XPS) spectra demonstrate that maintaining a reasonably high pH value (pH > 4) is an effective way to weaken H+ competition. This work provides a molecular-level understanding of adsorption sites, adsorption mechanism, and H+ competition for metal ion adsorption by PANI, which is beneficial for the development of PANI-based adsorbents. © 2023, The Authors. All rights reserved.

关键词： Adsorption

来源：评论

学校读者我要写书评

暂无评论

Adsorption of Dibenzofuran by Modified Biochar Derived from Microwave Gasification

SSRN

引用

SSRN 2024年

作者： Ren, Jiyun Zhang, Yong Wang, Hui Huang, Xiaoming Jin, Xiaoling Zhang, Kai Li, Ruiyu Yang, Kaixuan Yue, Yang Deng, Lei Che, Defu State Key Laboratory of Multiphase Flow in Power Engineering School of Energy and Power Engineering Xi’an Jiaotong University Xi’an710049 China Yantai Longyuan Power Technology Co. Ltd Yantai264000 China West Pipeline Company of PipeChina Urumchi830000 China Jinggangshan Power Plant Huaneng Power International Inc Jiangxi 343009 China Shunde Institute of Inspection Guangdong Institute of Special Equipment Inspection and Research Foshan528300 China Shanghai Power Equipment Research Institute Co. Ltd. Shanghai200240 China

Dioxins, emanating from the waste incineration, constitutes an organic pollutant that poses considerable risks to human health and environment. In this study, the corn straw char (CSC) and oak char (OC) derived from the electric heating and microwave gasification, and the coconut-shell activated carbon (AC) are employed as absorbents for the adsorption of dibenzofuran (DBF, dioxins model compound). Characterization techniques including BET, X-ray CT, SEM-EDS, FTIR, and XPS are performed to identify the DBF adsorption mechanism on biochar. The results show that the biochar prepared by the microwave gasification has a more well-developed pore structure than that of the electric heating gasification. Higher porosity (16.94%) and lower mineral content (1.75%) are responsible for the effective adsorption of DBF onto AC. The adsorption capacity of CSC is proportional to the modified concentration of KOH. It is mainly ascribed to the decrement of carboxyl and lactone groups and the enhancement of alkaline functional groups on the biochar surface, which augments the hydrophobicity and π–π electron donor–acceptor (EDA) interaction. Instead, DBF adsorption capacity on the biochar is adversely affected by HNO3 modification. For all biochar samples, the corresponding maximum adsorption ratios are AC (87.11%) > KOH-modified CSC (77.14%) > unmodified CSC (49.11%) > unmodified OC (39.70%) > HNO3-modified CSC (36.09%). The adsorption mechanisms of DBF on the gasified biochar encompass pore filling, hydrophobicity, and π–π EDA interaction. A desirable adsorption capacity of DBF on the biochar prepared by the microwave gasification is attainable through augmenting the specific surface area while diminishing the oxygen-containing groups of the surface simultaneously. © 2024, The Authors. All rights reserved.

关键词： Potassium hydroxide

来源：评论

学校读者我要写书评

暂无评论

Atomic Nickel on Graphitic Carbon Nitride as a Visible Light-Driven Hydrogen Production Photocatalyst Studied by X-ray Spectromicroscopy

引用

ACS Sustainable Chemistry and engineering 2023年第14期11卷 5390-5399页

作者： Huang, Yu-Cheng Li, Yanrui Arul, K. Thanigai Ohigashi, Takuji Nga, Ta Thi Thuy Lu, Ying-Rui Chen, Chi-Liang Chen, Jeng-Lung Shen, Shaohua Pong, Way-Faung Dong, Chung-Li Chou, Wu-Ching Department of Electrophysics National Yang Ming Chiao Tung University Hsinchu30010 Taiwan Research Center for X-ray Science & Department of Physics Tamkang University New Taipei City25137 Taiwan International Research Center for Renewable Energy State Key laboratory of Multiphase Flow in Power Engineering Xi’an Jiaotong University Shaanxi Xi’an710049 China Photon Factory Institute of Materials Structure Science High Energy Accelerator Research Organization Tsukabu305-0801 Japan UVSOR Synchrotron Facility Institute for Molecular Science Okazaki444-8585 Japan National Synchrotron Radiation Research Center Hsinchu30010 Taiwan

The photocatalytic production of solar hydrogen through water splitting by graphitic carbon nitride (g-C3N4) has gained substantial interest due to its advantageous characteristics, such as eco-friendliness, wealth on the earth, favorable bandgap, and easy preparation. Nevertheless, the performance for photocatalytic overall water splitting has been significantly restricted owing to the rapid recombination of charge carriers and slow catalytic kinetics. This investigation demonstrates the utilization of a single-atom Ni-terminating agent to coordinate with the heptazine moieties of g-C3N4, resulting in the formation of a new electronic orbital. g-C3N4 with single-atom Ni-termination can achieve highly efficient photocatalytic overall water splitting into H2 and H2O2 upon visible light irradiation, without requiring the use of any additional cocatalysts. The underlying cause of the enhanced photocatalytic performance of single-atom Ni-incorporated g-C3N4 in hydrogen evolution reaction is identified using synchrotron X-ray spectroscopy and microscopy. The X-ray spectro-microscopic results discover that the new hybrid orbital that is critical for optimizing photocatalysis is associated with carbon defects. The atomic and electronic structures and the band gap of g-C3N4 are adjusted by the new hybrid orbital. Moreover, it synergistically enhances visible light absorption, thereby promoting the separation and transfer of photogenerated charge carriers. The single-atom Ni and the adjacent C atom are recognized as the active sites for water oxidation and reduction, respectively, supporting the efficient photocatalytic splitting of water via a two-electron transfer pathway. This study demonstrated a promising material design for promoting photocatalytic activity in solar energy conversion applications. © 2023 American Chemical Society

关键词： Electronic structure

来源：评论

学校读者我要写书评

暂无评论

Solution chemistry back‐contact FTO/hematite interface engineering for efficient photocatalytic water oxidation

引用

Chinese Journal of Catalysis 2022年第5期43卷 1247-1257页

作者： Karen Cristina Bedin Beatriz Mouriño Ingrid Rodríguez-Gutiérrez João Batista Souza Junior Gabriel Trindade dos Santos Jefferson Bettini Carlos Alberto Rodrigues Costa Lionel Vayssieres Flavio Leandro Souza The National Nanotechnology Laboratory(LNNANO) Brazilian Center for Research in Energy and Materials(CNPEM)Campinas 13083‐970Brazil Centro de Ciências Naturais e Humanas(CCNH) Federal University of ABC(UFABC)Santo André09210580Brazil Federal University of Rio Grande do Sul(UFRGS) Rio Grande do SulBrazil International Research Center for Renewable Energy(IRCRE) State Key Laboratory of Multiphase Flow in Power EngineeringSchool of Energy and Power EngineeringXi’an Jiaotong UniversityXi’an 710049ShaanxiChina

This work describes a simple yet powerful scalable solution chemistry strategy to create back‐contact rich interfaces between substrates such as commercial transparent conducting fluorine‐doped tin oxide coated glass(FTO)and photoactive thin films such as hematite for low‐cost water oxidation ***‐resolution electron microscopy(SEM,TEM,STEM),atomic force microscopy(AFM),elemental chemical mapping(EELS,EDS)and photoelectrochemical(PEC)investigations reveal that the mechanical stress,lattice mismatch,electron energy barrier,and voids between FTO and hematite at the back‐contact interface as well as short‐circuit and detrimental reaction between FTO and the electrolyte can be alleviated by engineering the chemical composition of the precursor solutions,thus increasing the overall efficiency of these low‐cost photoanodes for water oxidation reaction for a clean and sustainable generation of hydrogen from PEC water‐*** findings are of significant importance to improve the charge collection efficiency by minimizing electron‐hole recombination observed at back‐contact interfaces and grain boundaries in mesoporous electrodes,thus improving the overall efficiency and scalability of low‐cost PEC water splitting devices.

关键词： Nanostructure Iron oxide Water oxidation Photoanode Surface engineering Chemical synthesis

来源：评论

学校读者我要写书评

暂无评论

Research on a Poly-Generation System for Gas-Biochar-Heat-Electricity by Supercritical Water Gasification of Biomass Waste

SSRN

引用

SSRN 2024年

作者： Wang, Cui Jin, Hui School of Water and Environment Chang'an University Xi’an710054 China Key Laboratory of Subsurface Hydrology and Ecological Effect in Arid Region of the Ministry of Education Chang'an University Xi’an710054 China Key Laboratory of Eco-hydrology and Water Security in Arid and Semi-arid Regions of Ministry of Water Resources Chang’an University Xi’an710054 China State Key Laboratory of Multiphase Flow in Power Engineering Xi'an Jiaotong University Xi’an710049 China Ministry of Education of China Chongqing University Chongqing400044 China

Biomass energy is renewable and rich in the world, providing a solution for the shortage in fossil fuel and serious environmental pollution. Proposing efficient utilization method of biomass waste demands urgent attention. Supercritical water gasification (SCWG) process is a potential technology. In this work, a poly-generation system based on SCWG was developed to convert biomass waste to gas, biochar, heat and electricity. Firstly, mass, energy, and exergy flow were calculated at the typical condition. Subsequently, impact of various operating parameters, including gasification temperature, mass flowrate of preheated water, biomass concentration, on the hydrogen-rich syngas yield, generated electricity, thermodynamic performance of the system was investigated. The result demonstrated that the exergy loss primarily occurred on cooler, reactor, heat exchanger and preheater, accounting for more than 90% of total exergy loss under different conditions, arising from irreversible reaction, heat transfer and heat dissipation. Higher temperature, higher biomass concentration and more preheated water exerted a positive effect for hydrogen-rich gas production and supplied heat energy, while these parameters were disadvantageous to exergy efficiency. Biochar energy was primarily affected by biomass concentration. Energy efficiency increased with preheated water quantity and biomass concentration rising, and impact of biomass concentration was more significant. Conversely, evaluated gasification temperature displayed an adverse effect on energy efficiency. The maximal exergy efficiency reached about 58.3% at 550℃, biomass concentration of 33%, preheated water mass flowrate of 900 kg·h-1 © 2024, The Authors. All rights reserved.

关键词： Biomass

来源：评论

学校读者我要写书评

暂无评论

Investigation of Droplet Dynamic Behavior in Pemfcs Gas Diffusion Layer and Gas Channel with Micro-Ct and Lattice Boltzmann Method

SSRN

引用

SSRN 2024年

作者： Lv, Xuecheng Zhou, Zhifu Wu, Wei-Tao Wei, Lei Gao, Linsong Lyu, Jizu Hu, Chengzhi Li, Yang Li, Yubai Song, Yongchen Key Laboratory of Ocean Energy Utilization and Energy Conservation of Ministry of Education Dalian University of Technology Dalian116024 China State Key Laboratory of Multiphase Flow in Power Engineering Xi'an Jiaotong University Xi'An710049 China School of Mechanical Engineering Nanjing University of Science and Technology Nanjing210094 China Department of Mechanical and Energy Engineering Southern University of Science and Technology Shenzhen518055 China School of Mechanical Engineering and Mechanics Xiangtan University Xiangtan411105 China School of Mechanical Engineering Guangdong Ocean University Zhanjiang524088 China

This study reconstructed the 3D structure for the gas diffusion layer (GDL) of proton exchange membrane fuel cells (PEMFCs) using the micro-CT technique and investigated the dynamic behavior of droplets inside the multi-scale space of GDL and gas channel (GC) using the lattice Boltzmann method (LBM). The prediction model for droplet detachment at the GDL-GC interface was developed. The results indicate that there is a significant difference between the breakage location of the liquid bridge and the trajectory of the liquid droplet after detaching from the GDL-GC interface in the multi-scale space of GC and GDL, compared to the single-scale GC space where GDL is ignored. The increase in gas velocity and internal contact angle of the GDL contribute to reducing the droplet detachment volume and increasing the droplet detachment frequency. At the internal contact angle of 120º-140º, GDL exhibited the most efficient removal of liquid water. A contact angle smaller than this range would hinder the detachment of droplets in the GC, while a contact angle larger than this range would lead to the accumulation of liquid water in the GDL. The surface force generated by the connection of liquid bridges in the analytical model for critical droplet detachment forms an angle with the gas flow direction, with the characteristic length determining this force being the minimum diameter at the necking of the liquid bridge. © 2024, The Authors. All rights reserved.

关键词： Contact angle

来源：评论

学校读者我要写书评

暂无评论

Waterside Corrosion of M5 Alloy in Simulated Primary Coolant and Supercritical Water: Influences of Aqueous Environments

SSRN

引用

SSRN 2022年

作者： Jiang, Guanyu Liu, Lu Xu, Donghai Li, Yanhui Kuang, Wenjun Wang, Mingjun Key Laboratory of Thermo-Fluid Science & Engineering Ministry of Education School of Energy and Power Engineering Xi’an Jiaotong University Shaanxi Province Xi’an710049 China State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong University Xi'An710049 China State Key Laboratory of Multiphase Flow in Power Engineering Department of Nuclear Science and Technology Xi'an Jiaotong University Xi'An China

M5 alloy is highly potential to serve as cladding materials in nuclear reactors. In this work, corrosion characteristics of M5 alloy in lithiated/borated water and pure supercritical water were investigated, and influences of aqueous environments on the corrosion process were clarified. Oxide films formed on the alloy mainly consisted of m-ZrO2. In the coolant environment, Li+ and OH- shared a synergistic effect on the occurrence and acceleration of waterside corrosion. Boric acid can react with OH- to induce B-(OH) formation and participate in the generation of zirconium borate to alleviate the accelerated corrosion effect by LiOH. In supercritical water, M5 alloy showed weight loss due to localized oxide exfoliation, and dissolved oxygen resulted in serious pitting of the oxide film. The microcrack density and porosity were significantly larger than those in the coolant environment, and long transverse cracks parallel to the O/M interface existed. Oxide deposition in two environments was both observed, and the phenomenon was discussed. © 2022, The Authors. All rights reserved.

关键词： Coolants

来源：评论

学校读者我要写书评

暂无评论

Dynamic Analysis and Optimization of Heat Transfer Performance During Electrospray Cooling with Ethanol-R141b Mixture

SSRN

引用

SSRN 2022年

作者： Tian, Jiameng Kong, Lingwen Li, Bufa Wang, Junfeng Chen, Bin Xiong, Junhui School of Energy and Power Engineering Jiangsu University Zhenjiang212013 China State Key Laboratory of Multiphase Flow in Power Engineering Xi’an Jiaotong University Shaanxi Xi’an710049 China Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Zhejiang Ningbo315201 China

Electrospray (ES) cooling that relies on Coulomb forces for energy-efficient liquid atomization is promising to meet the requirement of high-heat-flux thermal dissipation for micro-sized electronics under relative low... 详细信息

关键词： Ethanol

来源：评论

学校读者我要写书评

暂无评论

Thermodynamic analysis on a heat-power decoupling system integrated with absorption heat pump

Thermodynamic analysis on a heat-power decoupling system int...

引用

2019 Canadian Society for Civil engineering Annual Conference, CSCE 2019

作者： Wang, Liyuan Liu, Ming Fu, Yue Liu, Jiping Yan, Junjie MOE Key Laboratory of Thermal Fluid Science Engineering School of Energy and Power Engineering Xi'an Jiaotong University Xi'an Shaanxi China State Key Laboratory of Multiphase Flow in Power Engineering School of Energy and Power Engineering Xi'an Jiaotong University Xi'an Shaanxi China

ISBN: (纸本)9780791883747

Because of the continuous expanding of the district heating, the heating load of combined heat and power(CHP) plants increases year by year. The minimum power load of CHP plant increases with the heating load due to the heat-power coupling mechanism. Therefore, heat-power decoupling is necessary to improve the operation flexibility for CHP units. Integrating the absorption heat pump(AHP) is an effective method to realize the heat-power decoupling. In this study, a 330MW CHP unit model and AHP model have been developed and validated. The performance of the heat-power decoupling and energy saving performance has been investigated by comparing the thermodynamic performance indicators. Results show that, the proposed system can increase the maximum heating load and decrease the power generation when the primary network return temperature is decreased. When the heating steam extraction is kept constant, with the increase of the primary network return water temperature, the heat generation efficiency and the standard coal consumption rate of heating increases, the coal consumption rate of power generation and the heating efficiency decreases. And the primary network return water temperature increases from 40 °C to 70 °C, the coal consumption rate of power generation decreases by 4.3 g/kWh, and the coal consumption rate of heating increases by 0.67 kg/GJ. Copyright © 2020 ASME.

关键词： Water temperature

来源：评论

学校读者我要写书评

暂无评论

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案：

请选择收藏分类：

通借通还

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：