Hui Li

State Grid Electric Power Research Institute, Nan-ching-hsü, Jiangxi Sheng, China

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Publications (898)1795.96 Total impact

  • [Show abstract] [Hide abstract]
    ABSTRACT: A carbon nano-fiber based conductive polymer (CNFP) film was fabricated by multi-scale carbon nano-fibers (10 ~ 200 nm) an in-situ filtrating casting process, due to the well-connected hierarchical microstructures and strong-wrapped assembling among carbon nano-fibers, the as-prepared CNFP presents excellent electrical conductivity, high thermo-electric performance and good mechanical properties. And the resistivity of the CNFP exhibited piecewise linear temperature-dependent characteristics within a certain temperature range (0 ~ 280 °C). Furthermore, based on excellent electric and thermo-electric properties, CNFP was employed as electric heating element to develop a novel self-deicing road system. This CNFP-based deicing system is consisted of CNFP as thermal source, an AlN-ceramic insulated encapsulation layer, a multiwall carbon nanotube (MWCNT)/cement-based thermal conduction layer and a thermally insulated substrate. Additionally, the MWCNT/cement-based composite, which was filled with 3% by weight MWCNT, was proposed as the thermal conduction layer because its thermal conduction properties are superior to those of cement with other fillers and to those of common cement-based composites. To ensure the efficient operation of the CNFP, an AlN-ceramic wafer (0.5 mm) was employed as the electro-insulated layer because of its favorable insulating and thermo-conductive properties. The constructed system was applied in deicing and field snow-thawing studies, in which the effects of ambient temperature, heat flux density and ice thickness on the deicing and snow-thawing performance of the self-deicing system were investigated. The efficiency, repeatability, cost and feasibility of the self-deicing road system in both deicing and snow-thawing applications were analyzed. Indices for evaluating the deicing or snow-thawing performance of the self-deicing road system were proposed and the optimal values for each parameter are presented. The results demonstrate the promise of CNFP as heating element of self-heating pavement on a wide application in deicing or snow-thawing for infrastructures, including pavement, highway, airport and bridge.
    Innovative Developments of Advanced Multifunctional Nanocomposites in Civil and Structural Engineering, Edited by K.J. Loh, S. Nagarajaiah, 01/2016: chapter Chapter 10; Woodhead Publishing: Cambridge, England.
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    ABSTRACT: Considering the harmful impact of food antioxidants on human bodies, thoroughly exposing their potential effects at the molecular level is important. In this study, the binding interactions of butylated hydroxyanisole (BHA), a phenolic antioxidant, and its different major metabolites tert-butylhydroquinone (TBHQ) and tert-butylbenzoquinone (TBQ) with lysozyme were examined via fluorescence, three-dimensional fluorescence, circular dichroism (CD), and ligand-protein docking studies. The three compounds caused strong quenching of lysozyme fluorescence by a static quenching mechanism but with different quenching efficiencies and different effects on the α-helix content of the lysozyme. The order of binding affinity of lysozyme for all test compounds is as follows: BHA>TBQ>TBHQ. Thermodynamic parameters indicated that hydrogen bonding and van der Waals forces perform dominant functions in the binding between these compounds and lysozyme. Furthermore, structure-affinity relationships between the model compounds and lysozyme were established on the basis of computational analyses. Copyright © 2015 Elsevier Ltd. All rights reserved.
    Food Chemistry 12/2015; 188. DOI:10.1016/j.foodchem.2015.05.013 · 3.26 Impact Factor
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    ABSTRACT: The binding mechanism of aripiprazole (APZ) with human serum albumin (HSA) in the absence and presence of three cyclodextrins (CyDs) (β-cyclodextrin, hydroxypropyl-β-cyclodextrin, and (2,6-di-O-methyl)-β-cyclodextrin) was studied by fluorescence, ultraviolet–visible absorption, nuclear magnetic resonance, and circular dichroism (CD) spectroscopy. The CD results revealed some degree of recovery of refolding caused by APZ after the addition of CyD. The Stern–Volmer quenching constant and binding constant of the APZ–HSA interaction were smaller in the presence of the three CyDs. The ultraviolet–visible absorption results indicated that APZ formed 1:1 complex with the three CyDs. The 1H NMR spectra of CyD showed chemical shift and resolution loss of proton after the addition of HSA. Molecular modeling studies showed that both APZ and CyD bind to HSA. The process was initiated through inclusion of free APZ molecules by CyD and the increase in steric hindrance of CyD–HSA binding.
    Carbohydrate Polymers 10/2015; 131:65-74. DOI:10.1016/j.carbpol.2015.05.037 · 3.92 Impact Factor
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    ABSTRACT: Metal-organic frameworks (MOFs) have been attracted considerable attention for their applications in gas storage/separation, adsorption as well as catalysis. In this study, a facile solvothermal method was employed to prepare MOFs and graphitic carbon nitride (g-C3N4) hybrids, and a g-C3N4/Ti-benzenedicarboxylate (MIL-125(Ti)) heterostructures photocatalyst was successfully synthesized. The as-obtained materials were characterized by field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), N2 adsorption–desorption isotherm, thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflection spectroscopy (UV–vis DRS), and photoluminescence (PL) spectroscopy. It is indicated that the hybrids have large surface area, mesoporous structure, thermal stability, and enhanced visible-light absorption. Compared with pure MIL-125(Ti) and g-C3N4, the composites exhibited more efficient photocatalytic performance for Rhodamine B degradation from aqueous solution under visible-light irradiation. The optimal g-C3N4 content in g-C3N4/MIL-125(Ti) composite was determined to be 7.0 wt%, and the corresponding photodegradation rate for RhB was 0.0624 min−1, about 2.1 and 24 times higher than that of pure g-C3N4 and MIL-125(Ti), respectively. The indirect dye photosensitization, the Ti3+–Ti4+ intervalence electron transfer, and the synergistic effect between MIL-125(Ti) and g-C3N4 were the three reasons for improved photo-degradation performance. Therefore, it is reasonable to believe that metal-free semiconductor/MOFs photocatalysts have great potentiality in environmental remediation.
    Applied Catalysis B Environmental 09/2015; 174. DOI:10.1016/j.apcatb.2015.03.037 · 6.01 Impact Factor
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    ABSTRACT: In this article, a flax fiber yarn was grafted with nanometer sized TiO2, and the effects on the tensile and bonding properties of the single fibers and unidirectional fiber reinforced epoxy plates were studied. The flax fiber yarn was grafted with nanometer sized TiO2 through immersion in nano-TiO2/KH560 suspensions under sonification. The measured grafting content of the nano-TiO2 ranged from 0.89 wt.% to 7.14 wt.%, dependent on the suspension concentration. With the optimized nano-TiO2 grafting content (∼2.34 wt.%), the tensile strength of the flax fibers and the interfacial shear strength to an epoxy resin were enhanced by 23.1% and 40.5%, respectively. The formation of Si–O–Ti and C–O–Si bonds and the presence of the nano-TiO2 particles on the fiber surfaces contributed to the property enhancements. Unidirectional flax fiber reinforced epoxy composite (Vf = 35.4%) plates prepared manually showed significantly enhanced flexural properties with the grafting of nano-TiO2.
    Composites Part A Applied Science and Manufacturing 09/2015; 76. DOI:10.1016/j.compositesa.2015.05.027 · 3.01 Impact Factor
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    ABSTRACT: Rapid, cost-effective, sensitive and specific analysis of biomolecules is important in the modern healthcare system. Here, a fluorescent biosensing platform based on the polydopamine nanospheres (PDANS) intergrating with Exonuclease III (Exo III) was developed. Due to the interaction between the ssDNA and the PDANS, the fluorescence of 6-carboxyfluorescein (FAM) labelled in the probe would been quenched by PDANS through FRET. While, in the present of the target DNA, the probe DNA would hybridize with the target DNA to form the double-strand DNA complex. Thus, Exo III could catalyze the stepwise removal of mononucleotides from 3'-terminus in the probe DNA, releasing the target DNA. As the FAM was released from the probe DNA, the fluorescence would no longer been quenched, led to the signal on. As one target DNA molecule could undergo a number of cycles to trigger the degradation of abundant probe DNA, Exo III-assisted target recycling would led to the amplification of the signal. The detection limit for DNA was 5pM, which was 20 times lower than that without Exo III. And the assay time was largely shortened due to the faster signal recovery kinetics. What is more, this target recycling strategy was also applied to conduct an aptamer-based biosensing platform. The fluorescence intensity was also enhanced for the assay of adenosine triphosphate (ATP). For the Exo III-assisted target recycling amplification, DNA and ATP were fast detected with high sensitivity and selectivity. This work provides opportunities to develop simple, rapid, economical, and sensitive biosensing platforms for biomedical diagnostics. Copyright © 2015. Published by Elsevier B.V.
    Biosensors & Bioelectronics 09/2015; 71. DOI:10.1016/j.bios.2015.04.029 · 6.45 Impact Factor
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    ABSTRACT: β-Cyclodextrin (β-CD) and 2,6-di-O-methyl-β-cyclodextrin (DM-β-CD) inclusion complexes with riluzole (RLZ) were prepared to improve water solubility and broaden potential pharmaceutical applications. CDs/RLZ inclusion complexes were confirmed via phase solubility studies, FT-IR spectroscopy, PXRD, DSC, (1)H NMR, and SEM. Phase solubility studies indicated that β-CD and DM-β-CD can form 1:1 inclusion complexes with RLZ, and the stability constants were 663.17 and 1609.07M(-1), respectively. Water solubility and dissolution rate of RLZ were significantly improved in complex forms, implying that the inclusion complexes may develop pharmaceutical applications. Preliminary in vitro cytotoxicity assay also showed that RLZ hepatotoxicity was not increased in the inclusion complexes. Copyright © 2015 Elsevier Ltd. All rights reserved.
    Carbohydrate Polymers 09/2015; 129:9-16. DOI:10.1016/j.carbpol.2015.04.046 · 3.92 Impact Factor
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    ABSTRACT: α-Cyperone, as the main constituent of Cyperus rotundus, is a sesquiterpene ketone. In this work, LigandFit and CDOCKER docking programs of Discovery Studio 3.1 were used to preliminarily estimate and further confirm the binding sites of α-cyperone. LigandFit results showed that α-cyperone is mainly bound in subdomain IIA. This finding was further confirmed by CDOCKER results. Site marker competitive experimental results also suggested that α-cyperone contains the same binding site as warfarin. Software simulation results further revealed that α-cyperone is mainly bound in subdomain IIA. Site marker competitive experiment results are consistent with simulation results. 3D fluorescence and CD spectroscopy results indicated that the native conformation of HSA molecule is affected by the presence of α-cyperone.
    Journal of Luminescence 08/2015; 164. DOI:10.1016/j.jlumin.2015.03.025 · 2.37 Impact Factor
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    ABSTRACT: In this article, a pultruded unidirectional basalt fiber-reinforced polymer (BFRP) plate was thermally aged at 135 °C and 300 °C for 4 h, and subsequently immersed in distilled water or strong alkaline solution (simulating concrete pore water, pH = 12.6–13) for 3 months. The variation of the tensile and interlaminar shear (ILSS) properties of the BFRP plates was studied. Thermal aging exhibited a slight effect on both the longitudinal tensile properties and the interlaminar shear strength, although thermal decomposition of the resin matrix started at 300 °C and brought in a high void content (4.8%). FTIR and DMTA results indicate that thermal aging lead to postcuring and oxidation of the resin matrix, leading to an increase of the glass transition temperatures. Thermal aging accelerated the degradation of the BFRP plates in distilled water or alkaline solution at 20, 40 and 60 °C. In the studied hash immersion conditions of 60 °C alkaline solution for 3 months, the unaged, 135 °C aged and 300 °C aged BFRP samples showed reduction in the tensile strength by 43.2%, 62.3% and 74.1%, respectively. The higher the thermal aging and immersion temperatures, the more deterioration of the mechanical properties occurred. Alkaline solution immersion showed more adverse effects compared to the distilled water. The detrimental effects of the thermal aging were attributed to the formation of voids and cracks through which water or alkaline solution tended to easily penetrate into the BFRPs. The degradation of the resin due to thermal aging and immersion was analyzed with dynamic mechanical thermal analysis and scanning electron microscopy analysis. The long term variation of the tensile strength of BFRPs was evaluated based on the Arrhenius equation.
    Composites Part B Engineering 08/2015; 77. DOI:10.1016/j.compositesb.2015.03.066 · 2.98 Impact Factor
  • Gao Ma, Hui Li
    Journal of Composites for Construction 08/2015; DOI:10.1061/(ASCE)CC.1943-5614.0000572 · 1.83 Impact Factor
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    ABSTRACT: A novel microemulsion electrokinetic chromatography (MEEKC) method for the simultaneous separation and quantitative determination of phenylpropanoid glycosides in Rhodiola L. was developed. The effects of many parameters influencing separation characteristics were optimized. Retention factor met rosarin Keywords: Capillary electrophoresis; microemulsion electrokinetic chromatography; phenylpropanoid glycosides; rhodiola; rosarin; rosavin; rosin Document Type: Research Article Publication date: August 1, 2015 More about this publication? Current Pharmaceutical Analysis publishes authoritative reviews, written by experts in the field on all the most recent advances in pharmaceutical and biomedical analysis. All aspects of the field are represented including drug analysis, analytical methodology and instrumentation. The journal is essential to all involved in pharmaceutical, biochemical and clinical analysis. $(document).ready(function() { var shortdescription = $(".originaldescription").text().replace(/\\&/g, '&').replace(/\\, '<').replace(/\\>/g, '>').replace(/\\t/g, ' ').replace(/\\n/g, ''); if (shortdescription.length > 350){ shortdescription = "" + shortdescription.substring(0,250) + "... more"; } $(".descriptionitem").prepend(shortdescription); $(".shortdescription a").click(function() { $(".shortdescription").hide(); $(".originaldescription").slideDown(); return false; }); }); ben/cpa/2015/00000011/00000003/art00011 dcterms_title,dcterms_description,pub_keyword 6 5 20 40 5 GA_googleFillSlot("Horizontal_banner_bottom");
    Current Pharmaceutical Analysis 08/2015; 11(3). DOI:10.2174/1573412911666150121231557 · 0.77 Impact Factor
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    ABSTRACT: Fiber reinforced polymer (FRP) composites with anhydride cured epoxy resin matrices are widely used in civil engineering (e.g., pultruded FRP plates and bars), and their thermal aging behavior is a concern when they are subjected to elevated temperatures (e.g., FRP chimney). In the present article, thermal aging of an epoxy resin matrix at 130 °C–160 °C for 30 days was performed, and the effects on the flexural properties, molecular structures, free volume fraction, and mechanical properties were investigated. FTIR spectroscopy indicated that oxidation and molecular rearrangement occurred in the skin of the epoxy samples during thermal aging. Dynamic mechanical thermal analysis (DMTA) further illustrates the dominant effect of the molecular rearrangement in the sample skin with a thickness less than 100 μm, leading to a new high temperature tan δ peak. The free volume fraction of the skin and the bulk epoxy sample was characterized by positron annihilation lifetime spectroscopy (PALS). The results indicate that a noticeable reduction of the apparent free volume fraction occurred in the sample skin, while the bulk sample was only slightly affected. The flexural results indicate that thermal aging obviously reduced the break strain, while the flexural strength was only slightly affected and the modulus increased.
    Polymer Degradation and Stability 08/2015; 118:111-119. DOI:10.1016/j.polymdegradstab.2015.04.017 · 2.63 Impact Factor
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    ABSTRACT: This study presents a novel auxiliary damping control strategy to depress subsynchronous resonance (SSR) oscillations in nearby turbine generators. In the proposed control strategy, SSR damping is achieved by adding turbine generator speed as a supplementary signal at the active power loop of the rotor-side converter (RSC) of doubly-fed induction generator (DFIG)-based wind farms. To design the SSR auxiliary damping controller, a transfer function between turbine generator speed and the output active power of the wind farms was introduced to derive the analytical expression of the damping coefficient. Then the damping effect of the active power of the DFIG-based wind farms was analyzed, and the phase range to obtain positive damping was determined. Next, the PID phase compensation parameters of the auxiliary damping controller were optimized by genetic algorithm to obtain the optimum damping in the entire subsynchronous frequency band. The last, the validity and effectiveness of the proposed auxiliary damping control were demonstrated on a modified version of the IEEE first benchmark model by time domain simulation analysis with the use of DigSILENT/PowerFactory.
    International Journal of Electrical Power & Energy Systems 07/2015; 69. DOI:10.1016/j.ijepes.2015.01.002 · 3.43 Impact Factor
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    ABSTRACT: A sensitive micellar electrokinetic chromatographic method with laser-induced fluorescence detection was developed for the determination of alendronate sodium (ALN) and pamidronate disodium (PAM) after derivatization with 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole. The developed method was first used for the determination of ALN and PAM in pharmaceutical preparations. After optimization, baseline separation of the analytes could be obtained in <10 min in a running buffer composed of 10 mM sodium borate and 30 mM sodium dodecyl sulfate (pH 9.0) at a voltage of 15 kV with 25°C cartridge temperature and the samples were injected by pressure (3447.5 Pa × 3 s). The method has linearity range of 0.05-70 µg/mL for the analytes (correlation coefficients: 0.9995 and 0.9997), the detection limits were 4 and 10 ng/mL for ALN and PAM, respectively. In intraday precision experiment, the relative standard deviation (RSD) values for migration time were 0.30% (ALN) and 0.27% (PAM), and the RSD values for peak areas were 1.19% (ALN) and 1.32% (PAM). The ranges of recovery were 95.5-101.8 and 94.6-105.3% for ALN and PAM, respectively. This method is not only rapid and accurate but also has the potential to be used for the quality control in pharmaceutical preparations of the two drugs. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email:
    Journal of chromatographic science 06/2015; DOI:10.1093/chromsci/bmv074 · 1.03 Impact Factor
  • Journal of Structural Engineering 06/2015; DOI:10.1061/(ASCE)ST.1943-541X.0001337 · 1.49 Impact Factor
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    ABSTRACT: We have performed scanning tunneling microscopy/spectroscopy (STM/STS) study and first-principles calculations to investigate the atomic structure and electronic properties of silicon nanoribbons (SiNRs) grown on Ag(110). Despite of the extensive research on SiNRs in the last decades, its atomic structure is still not fully understood so far. In this report we determine that the structure of SiNRs/Ag(110) is armchair silicene nanoribbon with reconstructed edges. Meanwhile, pronounced quantum well states (QWS) in SiNRs were observed and their energy spectrum was systematically measured. The QWS are due to the confinement of quasiparticles perpendicular to the nanoribbon and can be well explained by the theory of one-dimensional (1D) 'particle-in-a-box' model in quantum mechanics.
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    ABSTRACT: X-ray powder diffraction data, unit-cell parameters, and space group for DCT (C 12 H 12 Cl 2 N 6 O 4 S 2 • C 6 H 15 N) are reported [ a = 18.991(9) Å, b = 19.057(2) Å, c = 7.346(8) Å, α = β = γ = 90°, unit-cell volume V = 2659.05 Å 3 , Z = 4, and space-group P 2 1 2 1 2 1 ]. No detectable impurity was observed.
    Powder Diffraction 06/2015; DOI:10.1017/S0885715615000299 · 0.59 Impact Factor
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    ABSTRACT: Graphane is graphene fully hydrogenated from both sides, forming a 1x1 structure, where all C atoms are in sp3 configuration. In silicene, the Si atoms are in a mix-sp2/sp3 configuration, it is therefore natural to imagine silicane in analogue to graphane. However, monoatomic silicene sheet grown on substrates generally reconstructs into different phases, and only partially hydrogenated silicene with reconstructions had been reported before. In this report we produce half-silicane, where one Si sublattice is fully H-saturated and the other sublattice is intact, forming a perfect 1x1 structure. By hydrogenating various silicene phases on Ag(111) substrate, we found that only the (2r3x2r3)R30{\deg} phase can produce half-silicane. Interestingly, this phase was previous considered to be a highly defective or incomplete silicene structure. Our results indicate that the structure of (2r3x2r3)R30{\deg} phase involves a complete silicene-1x1 lattice instead of defective fragments, and the formation mechanism of half-silicane was discussed with the help of first principles calculations.
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    ABSTRACT: This study aimed to improve the water solubility and reduce the toxicity of chlorzoxazone via complexation with β-cyclodextrin (β-CD) and hydroxypropyl-β-cyclodextrin (HP-β-CD). Inclusion complexes between chlorzoxazone and the two cyclodextrins (CDs) were prepared by freeze-drying method. Formation of the complexes was confirmed by FT-IR, PXRD, 1H NMR, DSC, and SEM. The water solubility and dissolution rates of chlorzoxazone were significantly increased by complexation with the two CDs. Preliminary in vitro cytotoxicity tests showed that the complexes are less toxic to normal liver cells than free chlorzoxazone. In general, the HP-β-CD complex exhibited better dissolution properties than the β-CD complex in various dissolution media. Therefore, the HP-β-CD complex can be used to design novel formulations of chlorzoxazone.
    Carbohydrate Polymers 06/2015; DOI:10.1016/j.carbpol.2015.05.055 · 3.92 Impact Factor
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    ABSTRACT: Tumor-associated macrophages (TAMs) have been found to be associated with the progression and metastasis of breast cancer. To clarify the mechanisms underlying the crosstalk between TAMs and cancer stem cells (CSCs) in breast cancer recurrence and metastasis, we used a co-culture model of macrophages and apoptotic human breast cancer cell line MCF-7 cells to investigate the effects of TAMs on MCF-7 in vitro and in vivo. Macrophages co-cultured with apoptotic MCF-7 had increased tumor growth and metastatic ability in a nude mouse transplantation assay. The macrophages exposed to apoptotic cells also induce an increase in the proportion of CD44+/CD24- cancer stem-like cells, as well as their proliferative ability accompanied with an increase in mucin1 (MUC1) expression. During this process, macrophages secreted increased amounts of interleukin 6 (IL-6) leading to increased phosphorylation of signal transducers and activators of transcription 3 (STAT3), which likely explains the increased transcription of STAT3 target genes such as TGF-β1 and HIF-1α. Our results indicate that when cancer cells endure chemotherapy induced apoptosis, macrophages in their microenvironment can then activate cancer stem cells to promote cancer growth and metastasis by secreting IL-6, which activates STAT3 phosphorylation to regulate the transcription of its downstream target genes.
    International Journal of Molecular Sciences 06/2015; 16(6):11966-82. DOI:10.3390/ijms160611966 · 2.34 Impact Factor

Publication Stats

7k Citations
1,795.96 Total Impact Points


  • 2015
    • State Grid Electric Power Research Institute
      Nan-ching-hsü, Jiangxi Sheng, China
  • 2014–2015
    • Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
      Shanghai, Shanghai Shi, China
    • The Chinese University of Hong Kong
      • Department of Information Engineering
      Hong Kong, Hong Kong
    • Xidian University
      Ch’ang-an, Shaanxi, China
    • Shaoxing University
      Shao-hsing, Zhejiang Sheng, China
  • 2013–2015
    • Technical Institute of Physics and Chemistry
      Peping, Beijing, China
    • Sun Yat-Sen University
      Shengcheng, Guangdong, China
    • Beijing University of Technology
      Peping, Beijing, China
  • 2011–2015
    • Chongqing University
      • State Key Laboratory of Power Transmission Equipment and System Security and New Technology
      Ch’ung-ch’ing-shih, Chongqing Shi, China
    • Northeastern University (Shenyang, China)
      Feng-t’ien, Liaoning, China
    • East China University of Science and Technology
      Shanghai, Shanghai Shi, China
    • Zhejiang University
      • Department of Environmental Science
      Hang-hsien, Zhejiang Sheng, China
  • 2008–2015
    • Guangxi Medical University
      • Department of Cardiology
      Yung-ning, Guangxi Zhuangzu Zizhiqu, China
    • University of Jinan (Jinan, China)
      Chi-nan-shih, Shandong Sheng, China
    • Peking Union Medical College Hospital
      Peping, Beijing, China
    • South China Normal University
      Shengcheng, Guangdong, China
  • 2007–2015
    • Nanjing University
      • Department of Chemical Engineering
      Nan-ching, Jiangsu Sheng, China
    • China Earthquake Administration
      Peping, Beijing, China
    • Jimei University
      Amoy, Fujian, China
    • Peking University Health Science Center
      Peping, Beijing, China
    • China University of Mining Technology
      Wu-hsien, Jiangsu Sheng, China
  • 2005–2015
    • Fujian Normal University
      Fujiang, Heilongjiang Sheng, China
    • Northeast Forestry University
      Charbin, Heilongjiang Sheng, China
  • 2004–2015
    • Harbin Institute of Technology
      • • School of Civil Engineering
      • • Department of Transportation Engineering
      Charbin, Heilongjiang Sheng, China
    • Sichuan University
      • • Institute of Atomic and Molecular Physics
      • • College of Chemical Engineering
      • • Department of Chemical Engineering
      • • College of Life Sciences
      Hua-yang, Sichuan, China
    • Beijing Jiaotong University
      Peping, Beijing, China
  • 2003–2015
    • Peking University
      • • Shenzhen Graduate School
      • • Health Science Center
      • • School of Basic Medical Science
      • • School of Pharmaceutical Sciences
      Peping, Beijing, China
  • 2012–2014
    • Fujian Provincial Cancer Hospital
      Min-hou, Fujian, China
    • Dalian University of Technology
      • School of Civil & Hydraulic Engineering
      Dalian, Liaoning, China
    • University of Electronic Science and Technology of China
      • State Key Laboratory of Electronic Thin Films and Integrated Devices
      Hua-yang, Sichuan, China
    • Shanxi Normal University
      Saratsi, Shanxi Sheng, China
    • Mianyang Normal University
      Mien-yang-hsien, Sichuan, China
    • Southwest Jiaotong University
      • School of Information Science and Technology
      Hua-yang, Sichuan, China
  • 2011–2014
    • Hebei Medical University
      Chentow, Hebei, China
    • Central South University
      • Department of Chemistry Engineering
      Ch’ang-sha-shih, Hunan, China
    • Southeast University (China)
      Nan-ching-hsü, Jiangxi Sheng, China
  • 2008–2014
    • University of Nebraska at Lincoln
      • • Department of Chemistry
      • • Nebraska Center for Materials and Nanoscience
      Lincoln, Nebraska, United States
  • 2006–2014
    • Shanghai Jiao Tong University
      Shanghai, Shanghai Shi, China
    • Chinese Academy of Sciences
      • • Laboratory of Theoretical Condensed Matter Physics and Computational Materials Physics
      • • Division of Cell and Stem Cell Biology
      • • Institute of High Energy Physics
      Peping, Beijing, China
    • Beijing University of Chemical Technology
      Peping, Beijing, China
  • 2012–2013
    • Ruijin Hospital North
      Shanghai, Shanghai Shi, China
  • 2010–2013
    • Tianjin University
      T’ien-ching-shih, Tianjin Shi, China
    • China Pharmaceutical University
      • Division of Analytical Chemistry
      Nan-ching-hsü, Jiangxi Sheng, China
    • China Agriculture University-East
      Peping, Beijing, China
  • 2009–2013
    • Guangdong Center for Disease Control and Prevention
      Shengcheng, Guangdong, China
    • China Agricultural University
      • • College of Food Science and Nutritional Engineering
      • • College of Engineering
      Peping, Beijing, China
    • Renji Hospital
      Shanghai, Shanghai Shi, China
    • Huazhong University of Science and Technology
      • Department of Electronics and Information Engineering
      Wu-han-shih, Hubei, China
    • Michigan State University
      Ист-Лансинг, Michigan, United States
    • National University of Singapore
      • Department of Chemistry
      Tumasik, Singapore
  • 1999–2013
    • Beijing Medical University
      • • Department of Surgery
      • • School of Pharmaceutical Sciences
      Peping, Beijing, China
  • 2010–2012
    • Yantai University
      • Science and Engineering College of Chemistry and Biology
      Chifu, Shandong Sheng, China
  • 2008–2012
    • Hunan University
      • • College of Environmental Science and Engineering
      • • College of Chemistry and Chemical Engineering
      Ch’ang-sha-shih, Hunan, China
  • 2006–2011
    • Tsinghua University
      • Department of Architecture
      Beijing, Beijing Shi, China
  • 2005–2009
    • Chinese Academy of Medical Sciences
      • Institute of Basic Medical Sciences (IBMS)
      Peping, Beijing, China
  • 2006–2008
    • Shandong University
      • Department of Computer Science and Technology
      Chi-nan-shih, Shandong Sheng, China
  • 2006–2007
    • Iowa State University
      • Department of Chemistry
      Ames, IA, United States
  • 2004–2005
    • Second Military Medical University, Shanghai
      Shanghai, Shanghai Shi, China
  • 2002–2005
    • University of Iowa
      • Department of Chemistry
      Iowa City, Iowa, United States
    • School of Pharmaceutical Sciences of Shandong
      Chi-nan-shih, Shandong Sheng, China
  • 1999–2000
    • Fujian Teachers University
      Min-hou, Fujian, China
  • 1998–1999
    • Shanghai Institute of Health Sciences
      Shanghai, Shanghai Shi, China