Siye Tang
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
Siye Tang has a total of 22 co-authors. Here are the top co-authors by number of shared publications:
- Xin-Xiang Cao
Laboratory for Development & Application of Cold Plasma Technology, College of Chemistry and Chemical Engineering, Luoyang Normal University, Luoyang 471022, China
3 shared publications - Arash Mirjalili
Department of Chemistry, University of California, Riverside, CA 92521, USA
2 shared publications - Ben W. -L. Jang
Department of Chemistry, Texas A&M University-Commerce, Commerce, TX 75429-3011, USA
2 shared publications - Chunlai Yang
Laboratory for Development & Application of Cold Plasma Technology, College of Chemistry and Chemical Engineering, Luoyang Normal University, Luoyang 471022, China
1 shared publication Da–Zhuang Liu
College of Chemical Engineering , Zhengzhou University , No. 97, WenHua Road, Henan Province, Zhengzhou 450002, China
1 shared publication- Huijie Zhu
College of Civil Engineering, Luoyang Institute of Science and Technology, Luoyang 471023, China
1 shared publication
Latest Publications
- Open Access
- 1 January 2025
- Published by National Library of Serbia in Journal of the Serbian Chemical Society
- Vol. 90 (6) , 767-780
Catalytic performance of palladium/degraded chitosan for acetylene selective hydrogenation
The aim of this paper was to investigate the catalytic properties of palladium supported on chitosan catalysts. The effect of primitive chitosan and degraded chitosan on catalytic performance was compared. The structure, morphology, metal content and properties of the catalysts were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), inductively coupled plasma spectrometry (ICP), X-ray diffraction (XRD), Brunauer?Emmett?Teller (BET) method and X-ray photoelectron spectroscopy (XPS). The results showed that the catalytic performance of Pd/degraded chitosan was better than that of Pd/chitosan at a certain Pd load. Pd/degraded chitosan (degradation 4 h) catalyst exhibited excellent catalytic performance and stability. The acetylene conversion and ethylene selectivity, respectively, achieved 100 and 91 %. During 13.5 h, the acetylene conversion maintained 100 % and the ethylene selectivity decreased slightly from 88 to 71 %. Based on this study, it was demonstrated that Pd was successfully coordinated with chitosan; after degradation, the chitosan particles became smaller and had larger surface areas; these were conducive to improve the catalytic performance of Pd/degraded chitosan. Pd/degraded chitosan also had high selectivity at high conversion, greatly improving the characteristics of low selectivity at high conversion of traditional Pd-based catalysts.
- 1 January 2025
- Published by National Library of Serbia in Journal of the Serbian Chemical Society
- Vol. 90 (6) , 767-780
Open AccessCatalytic performance of palladium/degraded chitosan for acetylene selective hydrogenation
The aim of this paper was to investigate the catalytic properties of palladium supported on chitosan catalysts. The effect of primitive chitosan and degraded chitosan on catalytic performance was compared. The structure, morphology, metal content and properties of the catalysts were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), inductively coupled plasma spectrometry (ICP), X-ray diffraction (XRD), Brunauer?Emmett?Teller (BET) method and X-ray photoelectron spectroscopy (XPS). The results showed that the catalytic performance of Pd/degraded chitosan was better than that of Pd/chitosan at a certain Pd load. Pd/degraded chitosan (degradation 4 h) catalyst exhibited excellent catalytic performance and stability. The acetylene conversion and ethylene selectivity, respectively, achieved 100 and 91 %. During 13.5 h, the acetylene conversion maintained 100 % and the ethylene selectivity decreased slightly from 88 to 71 %. Based on this study, it was demonstrated that Pd was successfully coordinated with chitosan; after degradation, the chitosan particles became smaller and had larger surface areas; these were conducive to improve the catalytic performance of Pd/degraded chitosan. Pd/degraded chitosan also had high selectivity at high conversion, greatly improving the characteristics of low selectivity at high conversion of traditional Pd-based catalysts.
- Open Access
Design of Pd–Zn Bimetal MOF Nanosheets and MOF-Derived Pd3.9Zn6.1/CNS Catalyst for Selective Hydrogenation of Acetylene under Simulated Front-End Conditions
Novel zinc–palladium–porphyrin bimetal metal–organic framework (MOF) nanosheets were directly synthesized by coordination chelation between Zn(II) and Pd(II) tetra(4-carboxyphenyl)porphin (TCPP(Pd)) using a solvothermal method. Furthermore, a serial of carbon nanosheets supported Pd–Zn intermetallics (Pd–Zn-ins/CNS) with different Pd: Zn atomic ratios were obtained by one-step carbonization under different temperature using the prepared Zn-TCPP(Pd) MOF nanosheets as precursor. In the carbonization process, Pd–Zn-ins went through the transformation from PdZn (650 °C) to Pd3.9Zn6.1 (~950 °C) then to Pd3.9Zn6.1/Pd (1000 °C) with the temperature increasing. The synthesized Pd–Zn-ins/CNS were further employed as catalysts for selective hydrogenation of acetylene. Pd3.9Zn6.1 showed the best catalytic performance compared with other Pd–Zn intermetallic forms.
Open AccessDesign of Pd–Zn Bimetal MOF Nanosheets and MOF-Derived Pd3.9Zn6.1/CNS Catalyst for Selective Hydrogenation of Acetylene under Simulated Front-End Conditions
Novel zinc–palladium–porphyrin bimetal metal–organic framework (MOF) nanosheets were directly synthesized by coordination chelation between Zn(II) and Pd(II) tetra(4-carboxyphenyl)porphin (TCPP(Pd)) using a solvothermal method. Furthermore, a serial of carbon nanosheets supported Pd–Zn intermetallics (Pd–Zn-ins/CNS) with different Pd: Zn atomic ratios were obtained by one-step carbonization under different temperature using the prepared Zn-TCPP(Pd) MOF nanosheets as precursor. In the carbonization process, Pd–Zn-ins went through the transformation from PdZn (650 °C) to Pd3.9Zn6.1 (~950 °C) then to Pd3.9Zn6.1/Pd (1000 °C) with the temperature increasing. The synthesized Pd–Zn-ins/CNS were further employed as catalysts for selective hydrogenation of acetylene. Pd3.9Zn6.1 showed the best catalytic performance compared with other Pd–Zn intermetallic forms.
- Open Access
Novel and Green Synthesis of Nitrogen-Doped Carbon Cohered Fe3O4 Nanoparticles with Rich Oxygen Vacancies and Its Application
A one-pot and green synthesis methodology was successfully designed to prepare nitrogen-doped carbon (NC) cohered Fe3O4 nanoparticles with rich oxygen vacancies (Fe3O4-OVs/NC). The preparation was achieved via cold-atmospheric-pressure air plasma using Fe2O3 nanoparticles as the only precursor, and pyridine as the carbon and nitrogen source. Systematic characterization results of the as-prepared Fe3O4-OVs/NC confirmed the transition from Fe2O3 to Fe3O4, along with the generation of oxygen vacancies, while preserving the original needle-like morphology of Fe2O3. Moreover, the results indicated the formation of the NC attaching to the surface of the formed Fe3O4 nanoparticles with a weight percent of ~13.6%. The synthesized nanocomposite was further employed as a heterogeneous Fenton catalyst to remove phenol from an aqueous solution. The material has shown excellent catalytic activity and stability, demonstrating a promising application for wastewater treatment.
Open AccessNovel and Green Synthesis of Nitrogen-Doped Carbon Cohered Fe3O4 Nanoparticles with Rich Oxygen Vacancies and Its Application
A one-pot and green synthesis methodology was successfully designed to prepare nitrogen-doped carbon (NC) cohered Fe3O4 nanoparticles with rich oxygen vacancies (Fe3O4-OVs/NC). The preparation was achieved via cold-atmospheric-pressure air plasma using Fe2O3 nanoparticles as the only precursor, and pyridine as the carbon and nitrogen source. Systematic characterization results of the as-prepared Fe3O4-OVs/NC confirmed the transition from Fe2O3 to Fe3O4, along with the generation of oxygen vacancies, while preserving the original needle-like morphology of Fe2O3. Moreover, the results indicated the formation of the NC attaching to the surface of the formed Fe3O4 nanoparticles with a weight percent of ~13.6%. The synthesized nanocomposite was further employed as a heterogeneous Fenton catalyst to remove phenol from an aqueous solution. The material has shown excellent catalytic activity and stability, demonstrating a promising application for wastewater treatment.
- 1 October 2006
- Published by Taylor & Francis in Physics and Chemistry of Liquids
- Vol. 44 (5) , 531-542
Determination of three-dimensional solubility parameters of chlorinated polypropylene by ultrasonic degradation
The degradation reactions of chlorinated polypropylene (CPP) in toluene under ultrasonic irradiation were studied. The Mark–Houwink equation acquired from fractional precipitations was also suitable for estimating the molecular weight of degraded CPP. An objective standard was proposed for judging the solution behaviour of CPP in solvents by the study on the relative solubility of CPP before and after degradation. Then Hansen three-dimensional solubility parameters and the total parameter of CPP were obtained by optimization calculation in terms of the criterion proposed here. It was proved that the total parameter of CPP is creditable by the turbidity method. Compared to other standards, the result obtained from the proposed standard accorded well with the standard of complete miscibility suggested by Flory–Huggins for polymers and solvents as well as the objective reality. This standard may provide a reference for other polymers.
- 1 October 2006
- Published by Taylor & Francis in Physics and Chemistry of Liquids
- Vol. 44 (5) , 531-542
Determination of three-dimensional solubility parameters of chlorinated polypropylene by ultrasonic degradation
The degradation reactions of chlorinated polypropylene (CPP) in toluene under ultrasonic irradiation were studied. The Mark–Houwink equation acquired from fractional precipitations was also suitable for estimating the molecular weight of degraded CPP. An objective standard was proposed for judging the solution behaviour of CPP in solvents by the study on the relative solubility of CPP before and after degradation. Then Hansen three-dimensional solubility parameters and the total parameter of CPP were obtained by optimization calculation in terms of the criterion proposed here. It was proved that the total parameter of CPP is creditable by the turbidity method. Compared to other standards, the result obtained from the proposed standard accorded well with the standard of complete miscibility suggested by Flory–Huggins for polymers and solvents as well as the objective reality. This standard may provide a reference for other polymers.