Catalytic activities of NiMo/MCM-41 and the mixture of Ni/MCM-41 with H-MCM-41 in cracking used ULO (lubricant oil) have been studied. This work was started by synthesis of aluminosilicate (MCM-41) at ratio of Si/...Catalytic activities of NiMo/MCM-41 and the mixture of Ni/MCM-41 with H-MCM-41 in cracking used ULO (lubricant oil) have been studied. This work was started by synthesis of aluminosilicate (MCM-41) at ratio of Si/AI = 50, using CTAB (cetyltrimethylammonium bromide) as a template, and TMAOH (tetramethylammonium hydroxide) as co-surfactant, where a hydrothermal process at 100 ℃ was conducted for 12 h. Organic compounds were then burned out from the dry solid material by calcination at 540 ℃. Ni/MCM-41 and H-MCM-41 were produced by ion exchange method, followed by reduction and calcination treatments, respectively, while NiMo/MCM-41 was produced by impregnation method followed by calcination. Product of MCM-41 was characterized by XRD (X-ray Diffraction), Fourier FTIR (transform infra red spectrophotometric), TEM (transmission electron microscopic) and BET (brunauer-emmet-teller) methods. Performance of the catalytic activities were shown by both of NiMo/MCM-41 and the mixture of 1:1 of H-MCM-41 and Ni/MCM-41 were mixed with the ULO at ratio of 1:200 (w/v) in a stainless steel reactor, then they were heated at 420 ℃. The products of cracking were analyzed using GC-MS (gas chromatography-mass spectrometry). Results of the work showed that the MCM-41 was successfully synthesized. Using mixture of Ni/MCM-41 and H-MCM-41 catalysts, 56.6% of ULO could be converted to OLP (organic liquid product). However, using NiMo/MCM-41 catalyst only 28.5% OLP could be produced. GC-MS analyses showed that cracking of the ULO at 420 ~C using NiMo/MCM-41 catalyst gave conversion 4.3% and 8.8% to gasoline like and diesel like fractions, respectively, while using mixture of Ni/MCM-41 and H-MCM-41 catalysts, conversion of 12.2% and 14.8% respectively to gasoline like and diesel like fractions were obtained.展开更多
This work presents a synthesis of bimetallic NiMo and NiW modified ZSM-5/MCM-41 composites and their heterogeneous catalytic conversion of crude palm oil( CPO) to biofuels. The ZSM-5/MCM-41 composites were synthesized...This work presents a synthesis of bimetallic NiMo and NiW modified ZSM-5/MCM-41 composites and their heterogeneous catalytic conversion of crude palm oil( CPO) to biofuels. The ZSM-5/MCM-41 composites were synthesized through a self-assembly of cetyltrimethylammonium bromide( CTAB) surfactant with silica-alumina from ZSM-5 zeolite,prepared from natural kaolin by the hydrothermal technique. Subsequently,the synthesized composites were deposited with bimetallic NiMo and NiW by impregnation method. The obtained catalysts presented a micro-mesoporous structure,confirmed by XRD,SEM,TEM,EDX,NH_3-TPD,XRF and N_2 adsorption-desorption measurements. The results of CPO conversion demonstrate that the catalytic activity of the synthesized catalysts decreases in the series of NiMo-ZSM-5/MCM-41 > NiW-ZSM-5/MCM-41 > Ni-ZSM-5/MCM-41 > Mo-ZSM-5/MCM-41 > W-ZSM-5/MCM-41 > NiMo-ZSM-5 > NiW-ZSM-5 > ZSM-5/MCM-41 > ZSM-5 > MCM-41. It was found that the bimetallic NiMo-and NiW-ZSM-5/MCM-41 catalysts give higher yields of liquid hydrocarbons than other catalysts at a given conversion. Types of hydrocarbon in liquid products,identified by simulated distillation gas chromatography-flame ionization detector( SimDis GC-FID),are gasoline( 150-200 ℃; C5-12),kerosene( 250-300 ℃; C5-20) and diesel( 350 ℃; C7-20).Moreover,the conversion of CPO to biofuel products using the NiMo-and NiW-ZSM-5/MCM-41 catalysts offers no statistically significant difference( P> 0.05) at 95% confidence level,evaluated by SPSS analysis.展开更多
文摘Catalytic activities of NiMo/MCM-41 and the mixture of Ni/MCM-41 with H-MCM-41 in cracking used ULO (lubricant oil) have been studied. This work was started by synthesis of aluminosilicate (MCM-41) at ratio of Si/AI = 50, using CTAB (cetyltrimethylammonium bromide) as a template, and TMAOH (tetramethylammonium hydroxide) as co-surfactant, where a hydrothermal process at 100 ℃ was conducted for 12 h. Organic compounds were then burned out from the dry solid material by calcination at 540 ℃. Ni/MCM-41 and H-MCM-41 were produced by ion exchange method, followed by reduction and calcination treatments, respectively, while NiMo/MCM-41 was produced by impregnation method followed by calcination. Product of MCM-41 was characterized by XRD (X-ray Diffraction), Fourier FTIR (transform infra red spectrophotometric), TEM (transmission electron microscopic) and BET (brunauer-emmet-teller) methods. Performance of the catalytic activities were shown by both of NiMo/MCM-41 and the mixture of 1:1 of H-MCM-41 and Ni/MCM-41 were mixed with the ULO at ratio of 1:200 (w/v) in a stainless steel reactor, then they were heated at 420 ℃. The products of cracking were analyzed using GC-MS (gas chromatography-mass spectrometry). Results of the work showed that the MCM-41 was successfully synthesized. Using mixture of Ni/MCM-41 and H-MCM-41 catalysts, 56.6% of ULO could be converted to OLP (organic liquid product). However, using NiMo/MCM-41 catalyst only 28.5% OLP could be produced. GC-MS analyses showed that cracking of the ULO at 420 ~C using NiMo/MCM-41 catalyst gave conversion 4.3% and 8.8% to gasoline like and diesel like fractions, respectively, while using mixture of Ni/MCM-41 and H-MCM-41 catalysts, conversion of 12.2% and 14.8% respectively to gasoline like and diesel like fractions were obtained.
基金The financial supported by Nakhon Ratchasima Rajabhat University,Nakhon Ratchasimathe National Research Council of Thailand+3 种基金Center of Excellence for Innovation in Chemistry (PERCH-CIC)Office of the Higher Education CommissionMinistry of Education and Materials Chemistry Research CenterDepartment of Chemistry Faculty of Science,Khon Kaen University,Thailand
文摘This work presents a synthesis of bimetallic NiMo and NiW modified ZSM-5/MCM-41 composites and their heterogeneous catalytic conversion of crude palm oil( CPO) to biofuels. The ZSM-5/MCM-41 composites were synthesized through a self-assembly of cetyltrimethylammonium bromide( CTAB) surfactant with silica-alumina from ZSM-5 zeolite,prepared from natural kaolin by the hydrothermal technique. Subsequently,the synthesized composites were deposited with bimetallic NiMo and NiW by impregnation method. The obtained catalysts presented a micro-mesoporous structure,confirmed by XRD,SEM,TEM,EDX,NH_3-TPD,XRF and N_2 adsorption-desorption measurements. The results of CPO conversion demonstrate that the catalytic activity of the synthesized catalysts decreases in the series of NiMo-ZSM-5/MCM-41 > NiW-ZSM-5/MCM-41 > Ni-ZSM-5/MCM-41 > Mo-ZSM-5/MCM-41 > W-ZSM-5/MCM-41 > NiMo-ZSM-5 > NiW-ZSM-5 > ZSM-5/MCM-41 > ZSM-5 > MCM-41. It was found that the bimetallic NiMo-and NiW-ZSM-5/MCM-41 catalysts give higher yields of liquid hydrocarbons than other catalysts at a given conversion. Types of hydrocarbon in liquid products,identified by simulated distillation gas chromatography-flame ionization detector( SimDis GC-FID),are gasoline( 150-200 ℃; C5-12),kerosene( 250-300 ℃; C5-20) and diesel( 350 ℃; C7-20).Moreover,the conversion of CPO to biofuel products using the NiMo-and NiW-ZSM-5/MCM-41 catalysts offers no statistically significant difference( P> 0.05) at 95% confidence level,evaluated by SPSS analysis.