资源类型

期刊论文 67

会议视频 1

年份

2024 1

2023 11

2022 6

2021 10

2020 2

2019 5

2018 4

2017 2

2016 4

2015 1

2014 2

2013 1

2012 1

2011 3

2010 2

2008 4

2007 5

2003 1

2001 1

2000 1

展开 ︾

关键词

合成橡胶 2

界面过渡区 2

/III-V界面 1

丙烯酰胺 1

乳液 1

二聚体 1

传递阻力 1

光热纱线 1

分子对接 1

分子设计 1

分子间力和表面力 1

动态荷载 1

反渗透 1

反相微乳液聚合 1

可调控供液 1

合成化学 1

复合树脂 1

太阳能界面海水淡化 1

孔结构 1

展开 ︾

检索范围：

排序： 展示方式：

The effect of altering crosslinker chemistry during interfacial polymerization on the performance of

《化学科学与工程前沿（英文）》 2023年 第17卷 第12期   页码 2025-2036 doi: 10.1007/s11705-023-2356-2

摘要： Chemistry of the polyamide active layer of a desalination membrane is critical in determining both its physical and chemical properties. In this study, we designed and fabricated three novel membranes with different active layers using the crosslinkers: terephthaloyl chloride, isophthaloyl chloride, and trimesoyl chloride. The crosslinkers were reacted with an aqueous solution of an aliphatic tetra-amine. Because these crosslinkers differ in their structures and crosslinking mechanisms during interfacial polymerization, the resultant membranes also possess different structural properties. The water contact angle of the fabricated membranes also varies; the water contact angles of 4A-3P-TPC@PSF/PET, 4A-3P-TMC@PSF/PET, and 4A-3P-IPC@PSF/PET, are 68.9°, 65.6°, and 53.9°, respectively. Similarly, the desalination performance of resultant membranes also showed variations, with 4A-3P-TPC@PSF/PET, 4A-3P-IPC@PSF/PET, and 4A-3P-TMC@PSF/PET having a permeate flux of 17.14, 25.70, and 30.90 L·m−2·h−1, respectively, at 2.5 MPa. The 4A-3P-TPC@PSF/PET membrane exhibited extensive crosslinking with aliphatic linear amine, and cationic dye rhodamine B, MgCl2, and amitriptyline rejection rates of 98.6%, 92.7% and 80.9%, respectively. The 4A-3P-TMC@PSF/PET membrane showed mediocre performance, while 4A-3P-IPC@PSF/PET membrane showed even lower performance, with a 35% rejection of methyl orange dye.

关键词： acid chlorides     covalent crosslinking     desalination     linear aliphatic amine     micropollutant removal     thin film composite membranes    

HTML PDF 收藏

Preparation and performance of novel thermal stable composite nanofiltration membrane

WU Chunrui, ZHANG Shouhai, YANG Fajie, YAN Chun, JIAN Xigao

《化学科学与工程前沿（英文）》 2008年 第2卷 第4期   页码 402-406 doi: 10.1007/s11705-008-0063-7

摘要： The novel thermal stable composite nanofiltration membranes were prepared through the interfacial polymerization of piperazine and trimesoyl chloride on the poly (phthalazinone ether) ultrafiltration substrate. The effects of polymerization and testing conditions on membrane performance were studied. The surface morphologies of the substrate and the composite membranes were observed by means of scanning electron microscopy (SEM) and atomic force microscopy (AFM). The separation properties of membranes for dyes and salts were tested. The composite membranes show good thermal stability. The rejection for NaSO was kept over 96%, while the flux reached 400 L·m·h when it was tested at 1.0 MPa and 80°C. When tested at 1.0 MPa and 60°C, the rejection of the composite membrane for dyes was kept at high level, and the flux reached 180–210 Lm·h, while the rejection for NaCl was lower than 20%.

关键词： electron microscopy     rejection     composite membrane     interfacial polymerization     thermal stability    

HTML PDF 收藏

Synthesis and characterization of castor oil-based polymeric surfactants

Xujuan HUANG,He LIU,Shibin SHANG,Zhaosheng CAI,Jie SONG,Zhanqian SONG

《农业科学与工程前沿（英文）》 2016年 第3卷 第1期   页码 46-54 doi: 10.15302/J-FASE-2016083

摘要： Dehydrated castor oil was epoxidized using phosphoric acid as a catalyst and acetic acid peroxide as an oxidant to produce epoxidized castor oil (ECO). Ring-opening polymerization with stannic chloride was used to produce polymerized ECO (PECO), and sodium hydroxide used to give hydrolyzed PECO (HPECO). The HPECO was characterized by Fourier transform infrared, H and C nuclear magnetic resonance spectroscopies, gel permeation chromatography, and differential scanning calorimetry. The weight-average molecular weight of soluble PECO and HPECO were 5026 and 2274 g·mol , respectively. PECO and HPECO exhibited glass transition. Through neutralizing the carboxylic acid of HPECO with different counterions, castor oil-based polymeric surfactants (HPECO-M, where M= Na , K or triethanolamine ion) exhibited high efficiency to reduce the surface tension of water. The critical micelle concentration (CMC) values of HPECO-M ranged from 0.042 to 0.098 g·L and the minimum equilibrium surface tensions at CMC ( ) of HPECO-M ranged from 25.6 to 30.0 mN·m . The water-hexadecane interfacial energy was calculated from measured surface tension using harmonic and geometric mean methods. Measured values of water-hexadecane interfacial tension agreed well with those calculated using the harmonic and geometric mean methods.

关键词： epoxidized vegetable oil     ring-opening polymerization     interfacial tension     polymeric surfactant    

HTML PDF 收藏

Preparation and properties of hollow fibre nanofiltration membrane with continuous coffee-ring structure

Xiuzhen Wei, Xufeng Xu, Yi Chen, Qian Zhang, Lu Liu, Ruiyuan Yang, Jinyuan Chen, Bosheng Lv

《化学科学与工程前沿（英文）》 2021年 第15卷 第2期   页码 351-362 doi: 10.1007/s11705-020-1943-8

摘要： Polyamide (PA) hollow fibre composite nanofiltration (NF) membranes with a coffee-ring structure and beneficial properties were prepared by adding graphene oxide (GO) into the interfacial polymerization process. The presentation of the coffee-ring structure was attributed to the heterogeneous, finely dispersed multiphase reaction system and the “coffee-stain” effect of the GO solution. When the piperazine concentration was 0.4 wt-%, the trimesoyl chloride concentration was 0.3 wt-%, and the GO concentration was 0.025 wt-%, the prepared NF membranes showed the best separation properties. The permeate flux was 76 L·m ·h , and the rejection rate for MgSO was 98.6% at 0.4 MPa. Scanning electron microscopy, atomic force microscopy, and attenuated total reflectance-Fourier transform infrared spectroscopy were used to characterize the chemical structure and morphology of the PA/GO NF membrane. The results showed that GO was successfully entrapped into the PA functional layer. Under neutral operating conditions, the PA/GO membrane showed typical negatively charged NF membrane separation characteristics, and the rejection rate decreased in the order of Na SO >MgSO >MgCl >NaCl. The PA/GO NF membrane showed better antifouling performance than the PA membrane.

关键词： GO     PA     interfacial polymerization     hollow fibre NF membrane    

HTML PDF 收藏

The effects of interfacial strength on fractured microcapsule

Luthfi Muhammad MAULUDIN, Chahmi OUCIF

《结构与土木工程前沿（英文）》 2019年 第13卷 第2期   页码 353-363 doi: 10.1007/s11709-018-0469-3

摘要： The effects of interfacial strength on fractured microcapsule are investigated numerically. The interaction between crack and microcapsule embedded in mortar matrix is modeled based on cohesive approach. The microcapsules are modelled with variation of core-shell thickness ratio and potential cracks are represented by pre-inserted cohesive elements along the element boundaries of the mortar matrix, microcapsules core, microcapsule shell, and at the interfaces between these phases. Special attention is given to the effects of cohesive fracture on the microcapsule interface, namely fracture strength, on the load carrying capacity and fracture probability of the microcapsule. The effect of fracture properties on microcapsule is found to be significant factor on the load carrying capacity and crack propagation characteristics. Regardless of core-shell thickness ratio of microcapsule, the load carrying capacity of self-healing material under tension increases as interfacial strength of microcapsule shell increases. In addition, given the fixed fracture strength of the interface of microcapsule shell, the higher the ratio core-shell thickness, the higher the probability of microcapsules being fractured.

关键词： interfacial strength     cohesive elements     microcapsule     core-shell thickness ratio     fracture properties    

HTML PDF 收藏

Effect of adding a smart potassium ion-responsive copolymer into polysulfone support membrane on the performance of thin-film composite nanofiltration membrane

Meibo He, Zhuang Liu, Tong Li, Chen Chen, Baicang Liu, John C. Crittenden

《化学科学与工程前沿（英文）》 2019年 第13卷 第2期   页码 400-414 doi: 10.1007/s11705-018-1757-0

摘要： Thin-film composite (TFC) nanofiltration (NF) membranes were fabricated via the interfacial polymerization of piperazine (PIP) and 1,3,5-benzenetricarbonyl trichloride on polysulfone (PSf) support membranes blended with K -responsive poly( -isopropylacryamide-co-acryloylamidobenzo-15-crown-5) (P(NIPAM-co-AAB C )). Membranes were characterized by attenuated total reflection Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, atomic force microscope, scanning electron microscope, contact angle, and filtration tests. The results showed that: (1) Under K -free conditions, the blended P(NIPAM-co-AAB C )/PSf supports had porous and hydrophilic surfaces, thereby producing NF membranes with smooth surfaces and low MgSO rejections; (2) With K in the PIP solution, the surface roughness and water permeability of the resultant NF membrane were increased due to the K -induced transition of low-content P(NIPAM-co-AAB C ) from hydrophilic to hydrophobic; (3) After a curing treatment at 95 °C, the improved NF membrane achieved an even higher pure water permeability of 10.97 L·m ·h ·bar under 200 psi. Overall, this study provides a novel method to improve the performance of NF membranes and helps understand the influence of supports on TFC membranes.

关键词： nanofiltration     interfacial polymerization     support membrane     potassium ion-responsive     thin-film composite    

HTML PDF 收藏

Construction of interfacial dynamic bonds for high performance lignin/polymer biocomposites

《化学科学与工程前沿（英文）》 2023年 第17卷 第10期   页码 1372-1388 doi: 10.1007/s11705-023-2302-3

摘要： Lignin is the largest natural aromatic biopolymer, but usually treated as industrial biomass waste. The development of lignin/polymer biocomposites can promote the high value utilization of lignin and the greening of polymers. However, the weak interfacial interaction between industrial lignin and polymer induces poor compatibility and serious agglomeration in polymer owing to the strong intermolecular force of lignin. As such, it is extremely difficult to prepare high performance lignin/polymer biocomposites. Recently, we proposed the strategy of in situ construction of interfacial dynamic bonds in lignin/polymer composites. By taking advantage of the abundant oxygen-containing polar groups of lignin, we inserted dynamic bonding connection such as hydrogen bonds and coordination bonds into the interphase between lignin and the polymer matrix to improve the interfacial interactions. Meanwhile, the natural amphiphilic structure characteristics of lignin were utilized to construct the hierarchical nanophase separation structure in lignin/polymer composites. The persistent problems of poor dispersity and interfacial compatibility of lignin in the polymer matrix were effectively solved. The lignin-modified polymer composites achieved simultaneously enhanced strength and toughness. This concise review systematically summarized the recent research progress of our group toward building high-performance lignin/polymer biocomposites through the design of interfacial dynamic bonds (hydrogen bonds, coordination bonds, and dynamic covalent bonds) between lignin and different polymer systems (polar plastics, rubber, polyurethane, hydrogels, and other polymers). Finally, the future development direction, main challenges, and potential solutions of lignin application in polymers were presented.

关键词： lignin     polymer     interfacial dynamic bonds    

HTML PDF 收藏

Thin-film composite forward osmosis membranes with substrate layer composed of polysulfone blended with PEG or polysulfone grafted PEG methyl ether methacrylate

Baicang Liu,Chen Chen,Pingju Zhao,Tong Li,Caihong Liu,Qingyuan Wang,Yongsheng Chen,John Crittenden

《化学科学与工程前沿（英文）》 2016年 第10卷 第4期   页码 562-574 doi: 10.1007/s11705-016-1588-9

摘要： To advance commercial application of forward osmosis (FO), we investigated the effects of two additives on the performance of polysulfone (PSf) based FO membranes: one is poly(ethylene glycol) (PEG), and another is PSf grafted with PEG methyl ether methacrylate (PSf-g-PEGMA). PSf blended with PEG or PSf-g-PEGMA was used to form a substrate layer, and then polyamide was formed on a support layer by interfacial polymerization. In this study, NaCl (1 mol?L ) and deionized water were used as the draw solution and the feed solution, respectively. With the increase of PEG content from 0 to 15 wt-%, FO water flux declined by 23.4% to 59.3% compared to a PSf TFC FO membrane. With the increase of PSf-g-PEGMA from 0 to 15 wt-%, the membrane flux showed almost no change at first and then declined by about 52.0% and 50.4%. The PSf with 5 wt-% PSf-g-PEGMA FO membrane showed a higher pure water flux of 8.74 L?m ?h than the commercial HTI membranes (6–8 L?m ?h ) under the FO mode. Our study suggests that hydrophobic interface is very important for the formation of polyamide, and a small amount of PSf-g-PEGMA can maintain a good condition for the formation of polyamide and reduce internal concentration polarization.

关键词： thin-film composite     forward osmosis     amphiphilic copolymer     interfacial polymerization     poly(ethylene glycol)    

HTML PDF 收藏

Gas phase ethylene polymerization over SiO

Liuzhong LI, Aiyou HAO, Ruihua CHENG, Boping LIU

《化学科学与工程前沿（英文）》 2011年 第5卷 第1期   页码 89-95 doi: 10.1007/s11705-010-0558-x

摘要： Although an important industrial catalyst for producing high density polyethylene, the SiO -supported organosilyl chromate UCC S-2 catalyst has not been fully investigated compared with the SiO -supported oxo chromium Phillips catalyst. In this work, gas phase ethylene polymerization by S-2 catalysts (Cat-1, Cat-2, and Cat-3) was carried out in a high-speed stirred-autoclave reactor. The effects of temperature, time, and pressure on kinetics, activity, and product properties were studied. All kinetics were typical built-up types with slow decay. Compared to the simple physical mixtures of Cat-1 and Cat-2, Cat-3 showed higher activity and its product had a broader molecular weight distribution, indicating new active species induced during blending of Cat-1 and Cat-2 in -hexane. The innovation by a simple catalyst technology created a new application to meet market demands.

关键词： UCC S-2 catalyst     Al-alkyl co-catalyst     gas-phase ethylene polymerization     high density polyethylene    

HTML PDF 收藏

Surface modification of biomaterials by photochemical immobilization and photograft polymerization to

Yakai FENG, Haiyang ZHAO, Li ZHANG, Jintang GUO,

《化学科学与工程前沿（英文）》 2010年 第4卷 第3期   页码 372-381 doi: 10.1007/s11705-010-0005-z

摘要： Thrombus formation and blood coagulation are serious problems associated with blood contacting products, such as catheters, vascular grafts, artificial hearts, and heart valves. Recent progresses and strategies to improve the hemocompatibility of biomaterials by surface modification using photochemical immobilization and photograft polymerization are reviewed in this paper. Three approaches to modify biomaterial surfaces for improving the hemocompatibility, i.e., bioinert surfaces, immobilization of anticoagulative substances and biomimetic surfaces, are introduced. The biomimetic amphiphilic phosphorylcholine and Arg-Gly-Asp (RGD) sequence are the most effective and most often employed biomolecules and peptide sequence for improving hemocompatibility of material surfaces. The RGD sequence can enhance adhesion and growth of endothelial cells (ECs) on material surfaces and increase the retention of ECs under flow shear stress conditions. This surface modification is a promising strategy for biomaterials especially for cardiovascular grafts and functional tissue engineered blood vessels.

关键词： biomimetic amphiphilic     amphiphilic phosphorylcholine     endothelial     functional     biomaterial    

HTML PDF 收藏

Synthesis and bulk polymerization kinetics of monomer dehydroabietic acid-(2-acryloyloxy-ethoxy)-ethyl

Haibo ZHANG,Yanping YANG,He LIU,Jie SONG,Shibin SHANG,Zhanqian SONG

《农业科学与工程前沿（英文）》 2017年 第4卷 第1期   页码 97-105 doi: 10.15302/J-FASE-2016115

摘要： A bulk polymerization monomer dehydro- abietic acid-(2-acryloyloxy-ethoxy)-ethyl ester (DHA-DG-AC) was synthesized from dehydroabietic acid (DHA). The chemical structure of DHA-DG-AC was characterized by H NMR, C NMR, MS and FT-IR. The kinetics of the bulk polymerization of DHA-DG-AC was investigated by Differential Scanning Calorimeter (DSC). Two kinds of kinetic model (nth-order model and autocatalytic model) were used to investigate the polymerization process. The results showed that the experimental DSC curves were consistent with the computational data generated by the autocatalytic kinetic model, and the value of was 95.73 kJ·mol .

关键词： dehydroabietic acid     bulk polymerization     kinetics     autocatalytic kinetic model    

HTML PDF 收藏

Studies on the liquid-liquid interfacial mass transfer process using holographic interferometry

ZHAO Chaofan, ZHU Chunying, MA Youguang

《化学科学与工程前沿（英文）》 2008年 第2卷 第1期   页码 1-4 doi: 10.1007/s11705-008-0006-3

摘要： This paper aims at the interfacial phenomena of liquid-liquid mass transfer and its characteristic. By using the real-time holographic technique, the concentration distributions on the aqueous side were obtained according to holographic diagrams of mass transfer of ethanol through the interface of oil and water at different initial concentrations. Furthermore, the concentrations near the interface and the mass transfer coefficients were attained. A correlation of concentration near the interface to the concentration of the solute in the oil side was proposed. An approach of interfacial energy with solute concentration was established, and the calculated results are at good agreement with the experimental data. It is indicated that the liquid-liquid mass transfer process is approximately in accordance with two-film theory, the interfacial performance may be changed by the addition of the solute, and the interface of liquid-liquid is non-equilibrium thermodynamically during the mass transfer process.

关键词： liquid-liquid     different     real-time holographic     addition     transfer    

HTML PDF 收藏

Interfacial induction and regulation for microscale crystallization process: a critical review

《化学科学与工程前沿（英文）》 2022年 第16卷 第6期   页码 838-853 doi: 10.1007/s11705-021-2129-8

摘要： Microscale crystallization is at the frontier of chemical engineering, material science, and biochemical research and is affected by many factors. The precise regulation and control of microscale crystal processes is still a major challenge. In the heterogeneous induced nucleation process, the chemical and micro/nanostructural characteristics of the interface play a dominant role. Ideal crystal products can be obtained by modifying the interface characteristics, which has been proven to be a promising strategy. This review illustrates the application of interface properties, including chemical characteristics (hydrophobicity and functional groups) and the morphology of micro/nanostructures (rough structure and cavities, pore shape and pore size, surface porosity, channels), in various microscale crystallization controls and process intensification. Finally, possible future research and development directions are outlined to emphasize the importance of interfacial crystallization control and regulation for crystal engineering.

关键词： interfacial crystallization     heterogeneous nucleation     supersaturation     micro/nanostructure     process control and intensification    

HTML PDF 收藏

Controlling microbiological interfacial behaviors of hydrophobic organic compounds by surfactants in

ZHANG Dong,ZHU Lizhong

《环境科学与工程前沿（英文）》 2014年 第8卷 第3期   页码 305-315 doi: 10.1007/s11783-014-0647-z

摘要： Bioremediation of hydrophobic organic compounds (HOCs) contaminated soils involves several physicochemical and microbiological interfacial processes among the soil-water-microorganism interfaces. The participation of surfactants facilitates the mass transport of HOCs in both the physicochemical and microbiological interfaces by reducing the interfacial tension. The effects and underlying mechanisms of surfactants on the physicochemical desorption of soil-sorbed HOCs have been widely studied. This paper reviewed the progress made in understanding the effects of surfactant on microbiological interfacial transport of HOCs and the underlying mechanisms, which is vital for a better understanding and control of the mass transfer of HOCs in the biodegradation process. In summary, surfactants affect the microbiological interfacial behaviors of HOCs during three consecutive processes: the soil solution-microorganism sorption, the transmembrane process, and the intracellular metabolism. Surfactant could promote cell sorption of HOCs depending on the compatibility of surfactant hydrophile hydrophilic balance (HLB) with cell surface properties; while the dose ratio between surfactant and biologic mass (membrane lipids) determined the transmembrane processes. Although surfactants cannot easily directly affect the intracellular enzymatic metabolism of HOCs due to the steric hindrace, the presence of surfactants can indirectly enhanced the metabolism by increasing the substrate concentrations.

关键词： biodegradation     sorption     transmembrane transport     microbiological interfaces     surfactants    

HTML PDF 收藏

A state-of-the-art review on interfacial behavior between asphalt binder and mineral aggregate

Meng GUO, Yiqiu TAN, Linbing WANG, Yue HOU

《结构与土木工程前沿（英文）》 2018年 第12卷 第2期   页码 248-259 doi: 10.1007/s11709-017-0422-x

摘要： The interface between asphalt binder and mineral aggregate directly affects the service life of pavement because the defects and stress concentration occur more easily there. The interaction between asphalt binder and mineral aggregate is the main cause of forming the interface. This paper presents an extensive review on the test technologies and analysis methods of interfacial interaction, including molecular dynamics simulation, phase field approach, absorption tests, rheological methods and macro mechanical tests. All of the studies conducted on this topic clearly indicated that the interfacial interaction between asphalt binder and mineral aggregate is a physical-chemical process, and can be qualitatively characterized by microscopical technique (such as SEM and AFM), and also can be quantitatively evaluated by rheological methods and interfacial mechanical tests. Molecular dynamics simulation and phase field approach were also demonstrated to be effective methods to study the interfacial behavior and its mechanism.

关键词： Asphalt binder     Mineral aggregate     Interfacial behavior     Multiscale    

HTML PDF 收藏

标题 作者 时间 类型 操作

The effect of altering crosslinker chemistry during interfacial polymerization on the performance of

期刊论文

Preparation and performance of novel thermal stable composite nanofiltration membrane

WU Chunrui, ZHANG Shouhai, YANG Fajie, YAN Chun, JIAN Xigao

期刊论文

Synthesis and characterization of castor oil-based polymeric surfactants

Xujuan HUANG,He LIU,Shibin SHANG,Zhaosheng CAI,Jie SONG,Zhanqian SONG

期刊论文

Preparation and properties of hollow fibre nanofiltration membrane with continuous coffee-ring structure

Xiuzhen Wei, Xufeng Xu, Yi Chen, Qian Zhang, Lu Liu, Ruiyuan Yang, Jinyuan Chen, Bosheng Lv

期刊论文

The effects of interfacial strength on fractured microcapsule

Luthfi Muhammad MAULUDIN, Chahmi OUCIF

期刊论文

Effect of adding a smart potassium ion-responsive copolymer into polysulfone support membrane on the performance of thin-film composite nanofiltration membrane

Meibo He, Zhuang Liu, Tong Li, Chen Chen, Baicang Liu, John C. Crittenden

期刊论文

Construction of interfacial dynamic bonds for high performance lignin/polymer biocomposites

期刊论文

Thin-film composite forward osmosis membranes with substrate layer composed of polysulfone blended with PEG or polysulfone grafted PEG methyl ether methacrylate

Baicang Liu,Chen Chen,Pingju Zhao,Tong Li,Caihong Liu,Qingyuan Wang,Yongsheng Chen,John Crittenden

期刊论文

Gas phase ethylene polymerization over SiO

Liuzhong LI, Aiyou HAO, Ruihua CHENG, Boping LIU

期刊论文

Surface modification of biomaterials by photochemical immobilization and photograft polymerization to

Yakai FENG, Haiyang ZHAO, Li ZHANG, Jintang GUO,

期刊论文

Synthesis and bulk polymerization kinetics of monomer dehydroabietic acid-(2-acryloyloxy-ethoxy)-ethyl

Haibo ZHANG,Yanping YANG,He LIU,Jie SONG,Shibin SHANG,Zhanqian SONG

期刊论文

Studies on the liquid-liquid interfacial mass transfer process using holographic interferometry

ZHAO Chaofan, ZHU Chunying, MA Youguang

期刊论文

Interfacial induction and regulation for microscale crystallization process: a critical review

期刊论文

Controlling microbiological interfacial behaviors of hydrophobic organic compounds by surfactants in

ZHANG Dong,ZHU Lizhong

期刊论文

A state-of-the-art review on interfacial behavior between asphalt binder and mineral aggregate

Meng GUO, Yiqiu TAN, Linbing WANG, Yue HOU

期刊论文