Ruiyuan Tang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Ruiyuan Tang has a total of 22 co-authors. Here are the top co-authors by number of shared publications:
- Zhibing Shen
Xi’an Key Laboratory of Low-Carbon Utilization for High-Carbon Resources, Xi’an Shiyou University, Xi’an 710065, China
3 shared publications - Juntao Zhang
Xi’an Key Laboratory of Low-Carbon Utilization for High-Carbon Resources, College of Chemistry and Chemical Engineering, Xi’an Shiyou University, Xi’an 710065, China
2 shared publications - Chang Che
State Key Laboratory of Shale Oil and Gas Enrichment Mechanisms and Effective Develpment, State Center for Research and Development of Oil Shale Exploitation, Petroleum Exploration and Production Research Institute, SINOPEC, Beijing 100083, China
1 shared publication - Haiyan Jiang
College of Petroleum Engineering, Xi’an Shiyou University
1 shared publication - Haolong Ning
Xi’an Key Laboratory of Low-Carbon Utilization for High-Carbon Resources, College of Chemistry and Chemical Engineering, Xi’an Shiyou University, Xi’an 710065, China
1 shared publication Jianling Luo
Xian Shiyou Univ, Xian Key Lab Low Carbon Utilizat High Carbon Resou, Xian 710065, Peoples R China
1 shared publication
Latest Publications
- Open Access
Non-Supported Heteroatom Modification Molybdenum-Based Catalyst for Synthesis Low-Carbon Alcohols from Coal-Based Syngas
Amid growing concerns over fossil fuel depletion and environmental degradation, developing alternative energy sources is imperative. While MoS2-based catalysts are known for their syngas conversion activity, their selectivity toward alcohols remains limited. This study addresses this gap by developing Cu-promoted MoS2 catalysts to enhance alcohol synthesis. The results indicated that the introduction of copper significantly modulates the catalytic performance of MoS2. We demonstrate that incorporating Cu significantly modulates the catalytic properties of MoS2. The optimized catalyst with 9 wt% Cu loading exhibited a CO conversion of 17.9% and a markedly improved total alcohol selectivity of 46.4%, with a space-time yield of 67.6 mg·g−1·h−1. Although Cu addition slightly reduced CO conversion, it markedly improved alcohol selectivity by facilitating active site dispersion, suppressing Fischer-Tropsch side reactions, and stabilizing heteroatomic active phases. Finally, a catalytic mechanism for the synthesis of low-carbon alcohols from syngas on MoS2-based catalysts was proposed based on the catalyst analysis and reaction results.
Open AccessNon-Supported Heteroatom Modification Molybdenum-Based Catalyst for Synthesis Low-Carbon Alcohols from Coal-Based Syngas
Amid growing concerns over fossil fuel depletion and environmental degradation, developing alternative energy sources is imperative. While MoS2-based catalysts are known for their syngas conversion activity, their selectivity toward alcohols remains limited. This study addresses this gap by developing Cu-promoted MoS2 catalysts to enhance alcohol synthesis. The results indicated that the introduction of copper significantly modulates the catalytic performance of MoS2. We demonstrate that incorporating Cu significantly modulates the catalytic properties of MoS2. The optimized catalyst with 9 wt% Cu loading exhibited a CO conversion of 17.9% and a markedly improved total alcohol selectivity of 46.4%, with a space-time yield of 67.6 mg·g−1·h−1. Although Cu addition slightly reduced CO conversion, it markedly improved alcohol selectivity by facilitating active site dispersion, suppressing Fischer-Tropsch side reactions, and stabilizing heteroatomic active phases. Finally, a catalytic mechanism for the synthesis of low-carbon alcohols from syngas on MoS2-based catalysts was proposed based on the catalyst analysis and reaction results.
- Open Access
Utilization of Metal-Functionalized ZSM-5 for Methanol and Low-Carbon Hydrocarbon Coupling Aromatization
Aromatics assume a paramount role as indispensable organic chemical feedstock within diverse industrial domains. Simultaneously, the global aromatics market is scarce, particularly with the exorbitant demand for high-value aromatics. Generating aromatics via coal-based methanol and low-carbon hydrocarbon coupling reactions has become a novel green and sustainable development trajectory. In this study, HZSM-5 catalysts featuring different Si/Al ratios and active metal-functionalized modifications were utilized to explore the aromatization effect in light of the Si/Al ratio, types of active components, and metal-loading content in a fixed-bed reactor. The outcomes were that the conversion ratios for methanol and n-pentane attained 99.9% and 83.1%, respectively. Remarkably, an oil phase yield of 32.1% was accomplished, along with an aromatic content of approximately 74.2%, while xylene selectivity reached approximately 37.6% for the 1.0%-ZnO/ZSM-5 (50) catalyst. Ultimately, a reaction mechanism for the coupling of methanol and n-pentane to yield aromatics using a 1.0%-ZnO/ZSM-5(50) catalyst is postulated.
Open AccessUtilization of Metal-Functionalized ZSM-5 for Methanol and Low-Carbon Hydrocarbon Coupling Aromatization
Aromatics assume a paramount role as indispensable organic chemical feedstock within diverse industrial domains. Simultaneously, the global aromatics market is scarce, particularly with the exorbitant demand for high-value aromatics. Generating aromatics via coal-based methanol and low-carbon hydrocarbon coupling reactions has become a novel green and sustainable development trajectory. In this study, HZSM-5 catalysts featuring different Si/Al ratios and active metal-functionalized modifications were utilized to explore the aromatization effect in light of the Si/Al ratio, types of active components, and metal-loading content in a fixed-bed reactor. The outcomes were that the conversion ratios for methanol and n-pentane attained 99.9% and 83.1%, respectively. Remarkably, an oil phase yield of 32.1% was accomplished, along with an aromatic content of approximately 74.2%, while xylene selectivity reached approximately 37.6% for the 1.0%-ZnO/ZSM-5 (50) catalyst. Ultimately, a reaction mechanism for the coupling of methanol and n-pentane to yield aromatics using a 1.0%-ZnO/ZSM-5(50) catalyst is postulated.
- Open Access
Catalytic Conversion of Oil Shale over Fe or Ni Catalysts under Sub-Critical Water
Sub-critical water is an environment-friendly solvent. It is widely used for the extraction of various organic compounds. It can be used to dissolve and transport organic matter in oil shale. In this study, the conversion of oil shale was synergistically catalyzed by the addition of Fe or Ni to the Fe inherent in samples under sub-critical water conditions. Oil shale can be converted to gas, oil and residues of oil. Thermogravimetric (TG) analysis results presented that the weight loss of raw oil shale was up to 15.85%. After sub-critical water extraction, the weight loss rate of the residues was reduced to 8.41%. With the application of a metal catalyst, Fe or Ni, the weight loss of residues was further reduced to 7.43% and 6.57%, respectively. According to DTG curves, it was found that there were two weight-loss rate peaks. The decomposition process of kerogen in oil shale could be divided into two cracking processes. One is decomposed at a high velocity at around 420 °C, and another is decomposed at a low velocity at around 515 °C. Gas chromatography (GC) results of gas products indicated that Fe or Ni could contribute to producing normal alkanes, such as methane, ethane, propane, etc., which are produced by the hydrogenation of alkenes via hydrogen transfer during the conversion process of kerogen. Gas chromatography-mass spectrometry (GC–MS) was conducted to analyze the components of the liquid products. The results showed that n-alkanes, iso-alkane, oxygenated hydrocarbons and aromatic compounds were the major components of the kerogen cracking products. When Ni was introduced as a catalyst, the contents of aromatic compounds and oxygenated hydrocarbons in the liquid products were increased from 19.55% and 6.87% to 22.38% and 13.77%, respectively. This is due to the synergistic effect of the addition of Ni with the inherent Fe in oil shale under sub-critical water which ensures kerogen is more easily cracked to produce aromatic compounds and oxygenated hydrocarbons.
Open AccessCatalytic Conversion of Oil Shale over Fe or Ni Catalysts under Sub-Critical Water
Sub-critical water is an environment-friendly solvent. It is widely used for the extraction of various organic compounds. It can be used to dissolve and transport organic matter in oil shale. In this study, the conversion of oil shale was synergistically catalyzed by the addition of Fe or Ni to the Fe inherent in samples under sub-critical water conditions. Oil shale can be converted to gas, oil and residues of oil. Thermogravimetric (TG) analysis results presented that the weight loss of raw oil shale was up to 15.85%. After sub-critical water extraction, the weight loss rate of the residues was reduced to 8.41%. With the application of a metal catalyst, Fe or Ni, the weight loss of residues was further reduced to 7.43% and 6.57%, respectively. According to DTG curves, it was found that there were two weight-loss rate peaks. The decomposition process of kerogen in oil shale could be divided into two cracking processes. One is decomposed at a high velocity at around 420 °C, and another is decomposed at a low velocity at around 515 °C. Gas chromatography (GC) results of gas products indicated that Fe or Ni could contribute to producing normal alkanes, such as methane, ethane, propane, etc., which are produced by the hydrogenation of alkenes via hydrogen transfer during the conversion process of kerogen. Gas chromatography-mass spectrometry (GC–MS) was conducted to analyze the components of the liquid products. The results showed that n-alkanes, iso-alkane, oxygenated hydrocarbons and aromatic compounds were the major components of the kerogen cracking products. When Ni was introduced as a catalyst, the contents of aromatic compounds and oxygenated hydrocarbons in the liquid products were increased from 19.55% and 6.87% to 22.38% and 13.77%, respectively. This is due to the synergistic effect of the addition of Ni with the inherent Fe in oil shale under sub-critical water which ensures kerogen is more easily cracked to produce aromatic compounds and oxygenated hydrocarbons.