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增材制造 5

激光选区熔化 2

电子束 2

超材料 2

选区激光熔化 2

选择性激光熔化 2

CCS 1

CO2分离 1

HEMTs）；栅槽；数字湿法腐蚀；选择性湿法腐蚀 1

VO2薄膜 1

主动控制 1

五模材料 1

仅1吸收 1

介观尺度模型 1

介观模型 1

偶氮苯 1

光学透明 1

光纤激光器；纳米片；传统孤子 1

光纤激光器；被动锁模；可饱和吸收体；二硫化钛 1

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Spectral emittance measurements of micro/nanostructures in energy conversion: a review

Shiquan SHAN, Chuyang CHEN, Peter G. LOUTZENHISER, Devesh RANJAN, Zhijun ZHOU, Zhuomin M. ZHANG

《能源前沿（英文）》 2020年 第14卷 第3期   页码 482-509 doi: 10.1007/s11708-020-0693-0

摘要： Micro/nanostructures play a key role in tuning the radiative properties of materials and have been applied to high-temperature energy conversion systems for improved performance. Among the various radiative properties, spectral emittance is of integral importance for the design and analysis of materials that function as radiative absorbers or emitters. This paper presents an overview of the spectral emittance measurement techniques using both the direct and indirect methods. Besides, several micro/nanostructures are also introduced, and a special emphasis is placed on the emissometers developed for characterizing engineered micro/nanostructures in high-temperature applications (e.g., solar energy conversion and thermophotovoltaic devices). In addition, both experimental facilities and measured results for different materials are summarized. Furthermore, future prospects in developing instrumentation and micro/nanostructured surfaces for practical applications are also outlined. This paper provides a comprehensive source of information for the application of micro/nanostructures in high-temperature energy conversion engineering.

关键词： concentrating solar power (CSP)     emittance measurements     high temperature     micro/nanostructure     selective absorber     selective emitter     thermophotovoltaics (TPV)    

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Recent advances in selective acetylene hydrogenation using palladium containing catalysts

Alan J. McCue, James A. Anderson

《化学科学与工程前沿（英文）》 2015年 第9卷 第2期   页码 142-153 doi: 10.1007/s11705-015-1516-4

摘要： Recent advances with Pd containing catalysts for the selective hydrogenation of acetylene are described. The overview classifies enhancement of catalytic properties for monometallic and bimetallic Pd catalysts. Activity/selectivity of Pd catalysts can be modified by controlling particle shape/morphology or immobilisation on a support which interacts strongly with Pd particles. In both cases enhanced ethylene selectivity is generally associated with modifying ethylene adsorption strength and/or changes to hydride formation. Inorganic and organic selectivity modifiers (i.e., species adsorbed onto Pd particle surface) have also been shown to enhance ethylene selectivity. Inorganic modifiers such as TiO change Pd ensemble size and modify ethylene adsorption strength whereas organic modifiers such as diphenylsulfide are thought to create a surface template effect which favours acetylene adsorption with respect to ethylene. A number of metals and synthetic approaches have been explored to prepare Pd bimetallic catalysts. Examples where enhanced selectivity is observed are generally associated with decreased Pd ensemble size and/or hindering of the ease with which an unselective hydride phase is formed for Pd. A final class of bimetallic catalysts are discussed where Pd is not thought to be the primary reaction site but merely acts as a site where hydrogen dissociation and spillover occurs onto a second metal (Cu or Au) where the reaction takes place more selectively.

关键词： acetylene     ethylene     selective hydrogenation     palladium     bimetallic    

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Preparation of polysulfone-based block copolymer ultrafiltration membranes by selective swelling and

《化学科学与工程前沿（英文）》 2022年 第16卷 第5期   页码 745-754 doi: 10.1007/s11705-021-2038-x

摘要： Selective swelling of block copolymers of polysulfone-b-poly(ethylene glycol) is an emerging strategy to prepare new types of polysulfone ultrafiltration membranes. Herein, we prepared nanoporous polysulfone-b-poly(ethylene glycol) ultrafiltration membranes by selective swelling and further promoted their porosity and ultrafiltration performances by using CaCO3 nanoparticles as the sacrificial nanofillers. Different contents of CaCO3 nanoparticles were doped into the solution of polysulfone-b-poly(ethylene glycol), and thus obtained suspensions were used to prepare both self-supported and bi-layered composite structures. Selective swelling was performed on the obtained block copolymer structures in the solvent pair of ethanol/acetone, producing nanoporous membranes with poly(ethylene glycol) lined along pore walls. The CaCO3 nanoparticles dispersed in polysulfone-b-poly(ethylene glycol) were subsequently etched away by hydrochloric acid and the spaces initially occupied by CaCO3 provided extra pores to the block copolymer layers. The porosity of the membranes was increased with increasing CaCO3 content up to 41%, but further increase in the CaCO3 content led to partial collapse of the membrane. The sacrificial CaCO3 particles provided extra pores and enhanced the connectivity between adjacent pores. Consequently, the membranes prepared under optimized conditions exhibited up to 80% increase in water permeance with slight decrease in rejection compared to neat membranes without the use of sacrificial CaCO3 particles.

关键词： block copolymers     selective swelling     ultrafiltration     CaCO3 nanoparticles     sacrificial nanofillers    

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基于图案化 VO2薄膜的透明热可调微波吸收器 Article

陆振刚, 张怡蕾, 王赫岩, 夏超, 刘云菲, 豆书亮, 李垚, 谭久彬

《工程（英文）》 2023年 第29卷 第10期   页码 198-206 doi: 10.1016/j.eng.2022.10.005

摘要：

理想的透明微波吸收器具有高光学透过率和强微波吸收能力，但是若其吸收性能固定，则会限制微波吸收器的应用。本文提出了一种基于二氧化钒(VO2)薄膜的透明热可调微波吸收器。理论计算和实验结果表明，所提出的吸波器在620 nm波长处可以实现84.9%的高光学透过率，同时通过控制温度，15.06 GHz频点处的反射损耗可在-4.257 dB到-60.179 dB范围内调谐并且在523.75 K温度时实现近1吸收。同时，仅通过调控图案化VO2薄膜的占空比即可改变实现近1吸收时的温度。所提出的基于VO2薄膜的吸波器具有组成简单，光学透过率高，微波吸收性能热可调，调制深度大，温度调节范围可控等优点，因此有望应用于可调传感器、热发射器、调制器、热成像仪、辐射热测定器和光电器件中。

关键词： 可调微波吸收器     VO2薄膜     光学透明     仅1吸收     大调制深度    

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Highly efficient and selective removal of vanadium from tungstate solutions by microbubble floating-extraction

《化学科学与工程前沿（英文）》 2023年 第17卷 第5期   页码 581-593 doi: 10.1007/s11705-022-2235-2

摘要： Selective separation of dissolved tungsten and vanadium is of great significance for the utilization of the secondary resources of these elements. In this work, selective removal of vanadium from tungstate solutions via microbubble floating-extraction was systematically investigated. The results indicated that vanadium can be more easily mineralized over tungsten from tungstate solutions using methyl trioctyl ammonium chloride as mineralization reagent under weak alkaline conditions. Owing to the higher bubble and interface mass transfer rates, high-efficiency enrichment and deep separation of vanadium could be achieved easily. Additionally, the deep recovery of tungsten and vanadium from the floated organic phase could be easily realized using a mixed solution of sodium hydroxide and sodium chloride as stripping agents. The separation mechanism mainly included the formation of hydrophobic complexes, their attachment on the surface of rising bubbles, and their mass transfer at the oil–water interface. Under the optimal conditions, the removal efficiency of vanadium reached 98.5% with tungsten loss below 8% after two-stage microbubble floating-extraction. Therefore, the microbubble floating-extraction could be an efficient approach for separating selectively vanadium from tungstate solutions, exhibiting outstanding advantages of high separation efficiency and low consumption of organic solvents.

关键词： tungsten     vanadium     selective separation     reagent mineralization     microbubble floating-extraction    

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Mechanistic insights into the selective photocatalytic degradation of dyes over TiO/ZSM-11

《环境科学与工程前沿（英文）》 2023年 第17卷 第8期 doi: 10.1007/s11783-023-1701-5

摘要：

● TiO2/ZSM-11 was prepared by a facile solid state dispersion method.

关键词： Selective dye degradation     Photocatalysis     TiO2     ZSM-11     Chemisorption    

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Porous ultrathin-shell microcapsules designed by microfluidics for selective permeation and stimuli-triggered

《化学科学与工程前沿（英文）》   页码 1643-1650 doi: 10.1007/s11705-022-2201-z

摘要： Microcapsules are versatile delivery vehicles and widely used in various areas. Generally, microcapsules with solid shells lack selective permeation and only exhibit a simple release mode. Here, we use ultrathin-shell water-in-oil-in-water double emulsions as templates and design porous ultrathin-shell microcapsules for selective permeation and multiple stimuli-triggered release. After preparation of double emulsions by microfluidic devices, negatively charged shellac nanoparticles dispersed in the inner water core electrostatically complex with positively charged telechelic α,ω-diamino functionalized polydimethylsiloxane polymers dissolved in the middle oil shell at the water/oil interface, thus forming a porous shell of shellac nanoparticles cross-linked by telechelic polymers. Subsequently, the double emulsions become porous microcapsules upon evaporation of the middle oil phase. The porous ultrathin-shell microcapsules exhibit excellent properties, including tunable size, selective permeation and stimuli-triggered release. Small molecules or particles can diffuse across the shell, while large molecules or particles are encapsulated in the core, and release of the encapsulated cargos can be triggered by osmotic shock or a pH change. Due to their unique performance, porous ultrathin-shell microcapsules present promising platforms for various applications, such as drug delivery.

关键词： microcapsule     emulsion     microfluidics     selective permeation     stimuli-triggered release    

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Highly selective and green recovery of lithium ions from lithium iron phosphate powders with ozone

《化学科学与工程前沿（英文）》 2023年 第17卷 第6期   页码 749-758 doi: 10.1007/s11705-022-2261-0

摘要： Since lithium iron phosphate cathode material does not contain high-value metals other than lithium, it is therefore necessary to strike a balance between recovery efficiency and economic benefits in the recycling of waste lithium iron phosphate cathode materials. Here, we describe a selective recovery process that can achieve economically efficient recovery and an acceptable lithium leaching yield. Adjusting the acid concentration and amount of oxidant enables selective recovery of lithium ions. Iron is retained in the leaching residue as iron phosphate, which is easy to recycle. The effects of factors such as acid concentration, acid dosage, amount of oxidant, and reaction temperature on the leaching of lithium and iron are comprehensively explored, and the mechanism of selective leaching is clarified. This process greatly reduces the cost of processing equipment and chemicals. This increases the potential industrial use of this process and enables the green and efficient recycling of waste lithium iron phosphate cathode materials in the future.

关键词： lithium iron phosphate powder     stoichiometric number     selective leaching     lithium recovery    

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Shape selective catalysis in methylation of toluene: Development, challenges and perspectives

Jian Zhou, Zhicheng Liu, Yangdong Wang, Dejin Kong, Zaiku Xie

《化学科学与工程前沿（英文）》 2018年 第12卷 第1期   页码 103-112 doi: 10.1007/s11705-017-1671-x

摘要： Toluene methylation with methanol offers an alternative method to produce -xylene by gathering methyl group directly from C1 chemical sources. It supplies a “molecular engineering” process to realize directional conversion of toluene/methanol molecules by selective catalysis in complicated methylation system. In this review, we introduce the synthesis method of -xylene, the development history of methylation catalysts and reaction mechanism, and the effect of reaction condition in -selective technical process. If constructing -xylene as the single target product, the major challenge to develop -selective toluene methylation is to improve the -xylene selectivity without, or as little as possible, losing the fraction of methanol for methylation. To reach higher yield of -xylene and more methanol usage in methylation, zeolite catalyst design should consider improving mass transfer and afterwards covering external acid sites by surface modification to get short “micro-tunnels” with shape selectivity. A solid understanding of mass transfer will benefit realizing the aim of converting more methanol feedstock into -methyl group.

关键词： shape selective catalysis     methylation of toluene    

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Review of the crushing response of collapsible tubular structures

Vivek PATEL, Gaurav TIWARI, Ravikumar DUMPALA

《机械工程前沿（英文）》 2020年 第15卷 第3期   页码 438-474 doi: 10.1007/s11465-019-0579-1

摘要： Studies on determining and analyzing the crushing response of tubular structures are of significant interest, primarily due to their relation to safety. Several aspects of tubular structures, such as geometry, material, configuration, and hybrid structure, have been used as criteria for evaluation. In this review, a comprehensive analysis of the important findings of extensive research on understanding the crushing response of thin-walled tubular structures is presented. Advancements in thin-walled structures, including multi-cell tube, honeycomb and foam-filled, multi wall, and functionally graded thickness tubes, are also discussed, focusing on their energy absorption ability. An extensive review of experimentation and numerical analysis used to extract the deformation behavior of materials, such as aluminum and steel, against static and dynamic loadings are also provided. Several tube shapes, such as tubes of uniform and nonuniform (tapered) cross sections of circular, square, and rectangular shapes, have been used in different studies to identify their efficacy. Apart from geometric and loading parameters, the effects of fabrication process, heat treatment, and triggering mechanism on initiating plastic deformation, such as cutouts and grooves, on the surface of tubular structures are discussed.

关键词： monolithic structure     crashworthiness     energy absorber     static and dynamic loadings     multicellular tube structure     filled tube    

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Design and operational considerations for selective catalytic reduction technologies at coal-fired boilers

Jeremy J. SCHREIFELS, Shuxiao WANG, Jiming HAO

《能源前沿（英文）》 2012年 第6卷 第1期   页码 98-105 doi: 10.1007/s11708-012-0171-4

摘要： By the end of 2010, China had approximately 650 GW of coal-fired electric generating capacity producing almost 75% of the country’s total electricity generation. As a result of the heavy reliance on coal for electricity generation, emissions of air pollutants, such as nitrogen oxides (NO ), are increasing. To address these growing emissions, the Ministry of Environmental Protection (MEP) has introduced new NO emission control policies to encourage the installation of selective catalytic reduction (SCR) technologies on a large number of coal-fired electric power plants. There is, however, limited experience with SCR in China. It is therefore useful to explore the lessons from the use of SCR technologies in other countries. This paper provides an overview of SCR technology performance at coal-fired electric power plants demonstrating emission removal rates between 65% and 92%. It also reviews the design and operational challenges that, if not addressed, can reduce the reliability, performance, and cost-effectiveness of SCR technologies. These challenges include heterogeneous flue gas conditions, catalyst degradation, ammonia slip, sulfur trioxide (SO ) formation, and fouling and corrosion of plant equipment. As China and the rest of the world work to reduce greenhouse gas emissions, carbon dioxide (CO ) emissions from parasitic load and urea-to-ammonia conversion may also become more important. If these challenges are properly addressed, SCR can reliably and effectively remove up to 90% of NO emissions at coal-fired power plants.

关键词： nitrogen oxides (NOx)     coal     selective catalytic reduction (SCR)     air pollution control    

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Low-temperature selective catalytic reduction of NO with NH based on MnO-CeO/ACFN

SHEN Boxiong, LIU Ting, SHI Zhanliang, SHI Jianwei, YANG Tingting, ZHAO Ning

《化学科学与工程前沿（英文）》 2008年 第2卷 第3期   页码 325-329 doi: 10.1007/s11705-008-0053-9

摘要： MnO-CeO/ACFN were prepared by the impregnation method and used as catalyst for selective catalytic reduction of NO with NH at 80°C–150°C. The catalyst was characterized by N-BET, scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR). The fraction of the mesopore and the oxygen functional groups on the surface of activated carbon fiber (ACF) increased after the treatment with nitric acid, which was favorable to improve the catalytic activities of MnO-CeO/ACFN. The experimental results show that the conversion of NO is nearly 100% in the range 100°C–150°C under the optimal preparation conditions of MnO-CeO/ACFN. In addition, the effects of a series of performance parameters, including initial NH concentration, NO concentration and O concentration, on the conversion of NO were studied.

关键词： preparation     conversion     favorable     selective catalytic     MnO-CeO/ACFN    

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Multi-stage ammonia production for sorption selective catalytic reduction of NO

Chen ZHANG, Guoliang AN, Liwei WANG, Shaofei WU

《能源前沿（英文）》 2022年 第16卷 第5期   页码 840-851 doi: 10.1007/s11708-021-0797-1

摘要： Sorption selective catalytic reduction of nitrogen oxides (NOx) (sorption-SCR) has ever been proposed for replacing commercial urea selective catalytic reduction of NOx (urea-SCR), while only the single-stage sorption cycle is hitherto adopted for sorption-SCR. Herein, various multi-stage ammonia production cycles is built to solve the problem of relative high starting temperature with ammonia transfer (AT) unit and help detect the remaining ammonia in ammonia storage and delivery system (ASDS) with ammonia warning (AW) unit. Except for the single-stage ammonia production cycle with MnCl2, other sorption-SCR strategies all present overwhelming advantages over urea-SCR considering the much higher NOx conversion driven by the heat source lower than 100°C and better matching characteristics with low-temperature catalysts. Furthermore, the required mass of sorbent for each type of sorption-SCR is less than half of the mass of AdBlue for urea-SCR. Therefore, the multifunctional multi-stage sorption-SCR can realize compact and renewable ammonia storage and delivery with low thermal energy consumption and high NOx conversion, which brings a bright potential for efficient commercial de-NOx technology.

关键词： selective catalytic reduction (SCR)     nitrogen oxides (NOx)     ammonia     composite sorbent     chemisorption    

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Insight into the promotion mechanism of activated carbon on the monolithic honeycomb red mud catalyst for selective

《环境科学与工程前沿（英文）》 2021年 第15卷 第5期 doi: 10.1007/s11783-020-1337-7

摘要：

• Activated carbon was proposed to be an efficient accelerant for molded red mud catalyst.

关键词： NOx     Selective catalytic reduction     Iron-based catalyst     Red mud     Monolithic catalyst     Activated carbon    

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Selective pseudosolubilization capability of

Fei HUA, Hongqi WANG

《环境科学与工程前沿（英文）》 2013年 第7卷 第4期   页码 539-551 doi: 10.1007/s11783-013-0498-z

摘要： Pseudosolubilized ability of sp. DG17 on -alkanes, role of biosurfactants in -octadecane uptake and trans-membrane transport mechanism of -octadecane were studied by analyzing amount of pseudosolubilized oil components in water phase, and the fraction of radiolabeled C -octadecane in the broth and cell pellet. GC-MS results showed that pseudosolubilized oil components were mainly C to C of -alkanes. In -octadecane broth, pseudosolubilized -octadecane could be accumulated as long as pseudosolubilized rate was faster than mineralization rate of substrate, and the maximum concentration of pseudosolubilized -octadecane achieved to 45.37 mg·L . All of these results showed that sp. DG17 mainly utilized alkanes by directly contacting with pseudosolubilized small oil droplets in the water phase. Analysis of C amount in cell pellet revealed that an energy-dependent system mainly controlled the trans-membrane transport of -octadecane.

关键词： Pseudomonas     alkane     uptake     pseudosolubilization     trans-membrane transport    

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标题 作者 时间 类型 操作

Spectral emittance measurements of micro/nanostructures in energy conversion: a review

Shiquan SHAN, Chuyang CHEN, Peter G. LOUTZENHISER, Devesh RANJAN, Zhijun ZHOU, Zhuomin M. ZHANG

期刊论文

Recent advances in selective acetylene hydrogenation using palladium containing catalysts

Alan J. McCue, James A. Anderson

期刊论文

Preparation of polysulfone-based block copolymer ultrafiltration membranes by selective swelling and

期刊论文

基于图案化 VO2薄膜的透明热可调微波吸收器

陆振刚, 张怡蕾, 王赫岩, 夏超, 刘云菲, 豆书亮, 李垚, 谭久彬

期刊论文

Highly efficient and selective removal of vanadium from tungstate solutions by microbubble floating-extraction

期刊论文

Mechanistic insights into the selective photocatalytic degradation of dyes over TiO/ZSM-11

期刊论文

Porous ultrathin-shell microcapsules designed by microfluidics for selective permeation and stimuli-triggered

期刊论文

Highly selective and green recovery of lithium ions from lithium iron phosphate powders with ozone

期刊论文

Shape selective catalysis in methylation of toluene: Development, challenges and perspectives

Jian Zhou, Zhicheng Liu, Yangdong Wang, Dejin Kong, Zaiku Xie

期刊论文

Review of the crushing response of collapsible tubular structures

Vivek PATEL, Gaurav TIWARI, Ravikumar DUMPALA

期刊论文

Design and operational considerations for selective catalytic reduction technologies at coal-fired boilers

Jeremy J. SCHREIFELS, Shuxiao WANG, Jiming HAO

期刊论文

Low-temperature selective catalytic reduction of NO with NH based on MnO-CeO/ACFN

SHEN Boxiong, LIU Ting, SHI Zhanliang, SHI Jianwei, YANG Tingting, ZHAO Ning

期刊论文

Multi-stage ammonia production for sorption selective catalytic reduction of NO

Chen ZHANG, Guoliang AN, Liwei WANG, Shaofei WU

期刊论文

Insight into the promotion mechanism of activated carbon on the monolithic honeycomb red mud catalyst for selective

期刊论文

Selective pseudosolubilization capability of

Fei HUA, Hongqi WANG

期刊论文