Zhenyu Liu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Zhenyu Liu has a total of 38 co-authors. Here are the top co-authors by number of shared publications:
Hongxian Niu
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, PR China
3 shared publicationsShoujun Liu
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, PR China
3 shared publicationsZhenping Zhu
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, PR China
3 shared publicationsJ. Wang
2 shared publicationsJianli Yang
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, 27 Taoyuan Nan Road, Taiyuan, Shanxi 030001, People's Republic of China
2 shared publicationsBaoqing Li
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, P.O. Box 165, Taiyuan 030001, People's Republic of China
1 shared publication
Latest Publications
- 30 June 2008
- Published by Elsevier in Journal of Fuel Chemistry and Technology
- Vol. 36 (3) , 257-260
Distribution of V2O5 on activated cokes measured by chemical adsorption
- 30 June 2008
- Published by Elsevier in Journal of Fuel Chemistry and Technology
- Vol. 36 (3) , 257-260
Distribution of V2O5 on activated cokes measured by chemical adsorption
- 25 June 2008
- Published by Wiley in Chemical Engineering & Technology
- Vol. 31 (7) , 1056-1061
Heterogeneity of V2O5 Supported Cylindrical Activated Coke Used for SO2 Removal from Flue Gas
- 25 June 2008
- Published by Wiley in Chemical Engineering & Technology
- Vol. 31 (7) , 1056-1061
Heterogeneity of V2O5 Supported Cylindrical Activated Coke Used for SO2 Removal from Flue Gas
- 1 May 2005
- Published by Springer Nature in Catalysis Letters
- Vol. 101 (1-2) , 27-30
Effect of SO2 on a cordierite honeycomb supported CuO catalyst for NO reduction by NH3
- 1 May 2005
- Published by Springer Nature in Catalysis Letters
- Vol. 101 (1-2) , 27-30
Effect of SO2 on a cordierite honeycomb supported CuO catalyst for NO reduction by NH3
- 1 September 2004
- Published by Elsevier in IFAC Proceedings Volumes
- Vol. 37 (13) , 627-632
A moving horizon H∞ tracking scheme for wheeled mobile robots with actuator constraints
- 1 September 2004
- Published by Elsevier in IFAC Proceedings Volumes
- Vol. 37 (13) , 627-632
A moving horizon H∞ tracking scheme for wheeled mobile robots with actuator constraints
- 25 June 2003
- Published by Institute of Electrical and Electronics Engineers (IEEE)
- p. 311
Surface characterization and antibacterial adhesion of poly (ethylene terephthalate) modified by acetylene plasma immersion ion implantation
Summary form only given. This article reports a study of the behavior of bacterial adhesion to polyethylene terephthalate (PET) which was modified by acetylene (C/sub 2/H/sub 2/) plasma immersion ion implantation (PIII). These surface-modified PETs were characterized by means of X-ray photoelectron spectroscopy (XPS) and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FT IR). The capacities of Staphylococcus aureus (SA), Staphylococcus epidermidis (SE), Escherichia coli (EQ), Pseudomonas aeruginosa (PA) and Candida albicans (CA) for adhesion to PETs were quantitatively determined by the plate counting and Gamma-ray counting of /sup 125/I radio labeled bacteria in vitro. The results indicated that the capacities of five types of bacteria for adhesion to PETs were all suppressed by PHI treatment. The adhesion of SA on the surface of C/sub 2/H/sub 2/ PIII modified surface was reduced to 1/10 of that on the untreated PET surface. The capacities of SE on the modified surface were 25% comparing with that of the untreated surface. XPS and ATR-FTIR spectra showed amorphous carbon structure appeared after C/sub 2/H/sub 2/ plasma immersion ion implantation. This suggests that the improvement of bacterial adhesion to PET might come from the formation of an amorphous carbon phase by PHI. It is believed that the composition change of the modified surface layer would cause the improvement of the bacterial adhesion.
- 25 June 2003
- Published by Institute of Electrical and Electronics Engineers (IEEE)
- p. 311
Surface characterization and antibacterial adhesion of poly (ethylene terephthalate) modified by acetylene plasma immersion ion implantation
Summary form only given. This article reports a study of the behavior of bacterial adhesion to polyethylene terephthalate (PET) which was modified by acetylene (C/sub 2/H/sub 2/) plasma immersion ion implantation (PIII). These surface-modified PETs were characterized by means of X-ray photoelectron spectroscopy (XPS) and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FT IR). The capacities of Staphylococcus aureus (SA), Staphylococcus epidermidis (SE), Escherichia coli (EQ), Pseudomonas aeruginosa (PA) and Candida albicans (CA) for adhesion to PETs were quantitatively determined by the plate counting and Gamma-ray counting of /sup 125/I radio labeled bacteria in vitro. The results indicated that the capacities of five types of bacteria for adhesion to PETs were all suppressed by PHI treatment. The adhesion of SA on the surface of C/sub 2/H/sub 2/ PIII modified surface was reduced to 1/10 of that on the untreated PET surface. The capacities of SE on the modified surface were 25% comparing with that of the untreated surface. XPS and ATR-FTIR spectra showed amorphous carbon structure appeared after C/sub 2/H/sub 2/ plasma immersion ion implantation. This suggests that the improvement of bacterial adhesion to PET might come from the formation of an amorphous carbon phase by PHI. It is believed that the composition change of the modified surface layer would cause the improvement of the bacterial adhesion.
- 23 February 2001
- Published by Elsevier in Applied Catalysis B: Environment and Energy
- Vol. 30 (3-4) , 267-276
Catalytic NO reduction with ammonia at low temperatures on V2O5/AC catalysts: effect of metal oxides addition and SO2
- 23 February 2001
- Published by Elsevier in Applied Catalysis B: Environment and Energy
- Vol. 30 (3-4) , 267-276
Catalytic NO reduction with ammonia at low temperatures on V2O5/AC catalysts: effect of metal oxides addition and SO2
- 1 January 2001
- Published by Elsevier in Journal of Catalysis
- Vol. 197 (1) , 6-16
Mechanism of SO2 Promotion for NO Reduction with NH3 over Activated Carbon-Supported Vanadium Oxide Catalyst
- 1 January 2001
- Published by Elsevier in Journal of Catalysis
- Vol. 197 (1) , 6-16
Mechanism of SO2 Promotion for NO Reduction with NH3 over Activated Carbon-Supported Vanadium Oxide Catalyst
- 1 October 2000
- Published by Elsevier in Journal of Catalysis
- Vol. 195 (2) , 268-278
Decomposition and Reactivity of NH4HSO4 on V2O5/AC Catalysts Used for NO Reduction with Ammonia
- 1 October 2000
- Published by Elsevier in Journal of Catalysis
- Vol. 195 (2) , 268-278
Decomposition and Reactivity of NH4HSO4 on V2O5/AC Catalysts Used for NO Reduction with Ammonia