Catalytic Decomposition of CCl2F2 over Solid Base Na2O/ZrO2

2013 ◽  
Vol 634-638 ◽  
pp. 494-499
Author(s):  
Tian Cheng Liu ◽  
Ping Ning ◽  
Hong Bin Wang ◽  
Lin Zhuan Ma ◽  
Bin Li

Catalytic decomposition of dichlorodifluoromethane (CCl2F2) in the presence of water vapor and oxygen was studied over a series of solid base that have different ZrO2 content using a fixed-bed reactor. CO2 and CClF3 were the main-products and no CO was detected as by-product. The decomposition activity depended on the calcination temperature and the Zr:Na. Calcined at 600 °C and Zr:Na=1:0.35 were the best catalyst preparation conditions. Adopting low concentration of oxygen and CCl2F2 and high concentration of water vapor is preferable to the achievement of high conversion of CCl2F2 and selectivity for CO2. The catalytic activity of Na2O/ZrO2 remained steady for 120 h on stream.

2013 ◽  
Vol 652-654 ◽  
pp. 1533-1538
Author(s):  
Tian Cheng Liu ◽  
Ping Ning ◽  
Hong Bin Wang ◽  
Jun Ming Guo

Catalytic hydrolysis decomposition of dichlorodifluoromethane (CCl2F2) in the presence of water vapor and oxygen was studied over a series of solid base that have different ZrO2 content using a fixed-bed reactor. CO2 and CClF3 were the main-products and no CO was detected as by-product. The decomposition activity depended on the calcination temperature and the Zr:Ca. Calcined at 650 °C and Zr:Ca=1:0.35 were the best catalyst preparation conditions. Adopting low concentration of oxygen and CCl2F2 and high concentration of water vapor is preferable to the achievement of high conversion of CCl2F2 and selectivity for CO2. The catalytic activity of CaO/ZrO2 remained steady for 20 h on stream.


2013 ◽  
Vol 457-458 ◽  
pp. 112-115
Author(s):  
Tian Cheng Liu ◽  
Yu Jiao Guo ◽  
Guang Yang Tang ◽  
Ming Long Yuan ◽  
Ping Ning

Catalytic hydrolysis decomposition of dichlorodifluoromethane (CCl2F2) in the presence of water vapor and oxygen was studied over solid base Na2O/ZrO2 using a fixed-bed reactor. The CCl2F2 adsorption was multilayer chemical adsorption and its process was corresponding with Freundlich model. Its adsorption heat was from 43.74 to 76.31 KJ.mol-1, and the CCl2F2 adsorption over solid base Na2O/ZrO2 was exothermic and chemical.


Energies ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 3347
Author(s):  
Arslan Mazhar ◽  
Asif Hussain Khoja ◽  
Abul Kalam Azad ◽  
Faisal Mushtaq ◽  
Salman Raza Naqvi ◽  
...  

Co/TiO2–MgAl2O4 was investigated in a fixed bed reactor for the dry reforming of methane (DRM) process. Co/TiO2–MgAl2O4 was prepared by modified co-precipitation, followed by the hydrothermal method. The active metal Co was loaded via the wetness impregnation method. The prepared catalyst was characterized by XRD, SEM, TGA, and FTIR. The performance of Co/TiO2–MgAl2O4 for the DRM process was investigated in a reactor with a temperature of 750 °C, a feed ratio (CO2/CH4) of 1, a catalyst loading of 0.5 g, and a feed flow rate of 20 mL min−1. The effect of support interaction with metal and the composite were studied for catalytic activity, the composite showing significantly improved results. Moreover, among the tested Co loadings, 5 wt% Co over the TiO2–MgAl2O4 composite shows the best catalytic performance. The 5%Co/TiO2–MgAl2O4 improved the CH4 and CO2 conversion by up to 70% and 80%, respectively, while the selectivity of H2 and CO improved to 43% and 46.5%, respectively. The achieved H2/CO ratio of 0.9 was due to the excess amount of CO produced because of the higher conversion rate of CO2 and the surface carbon reaction with oxygen species. Furthermore, in a time on stream (TOS) test, the catalyst exhibited 75 h of stability with significant catalytic activity. Catalyst potential lies in catalyst stability and performance results, thus encouraging the further investigation and use of the catalyst for the long-run DRM process.


2013 ◽  
Vol 295-298 ◽  
pp. 326-330 ◽  
Author(s):  
Tian Cheng Liu ◽  
Yu Jiao Guo ◽  
Ping Ning ◽  
Ming Long Yuan

Catalytic hydrolysis decomposition of dichlorodifluoromethane (CCl2F2) in the presence of water vapor and oxygen was studied over a series of solid acids using a fixed-bed reactor. Solid acid MoO3/ZrO2 displayed the highest activity, over which the conversion of CCl2F2 reached 100 % at 250 °C. CO2 was the main-product and the selectivity to CClF3 remained lower than 28.0 %. CO was not detected as by-product. The decomposition activity depended on the calcination temperature and the ZrO2 content. The activity of solid acid MoO3/ZrO2 correlates well with its specific surface area and the amount of medium-strong acid sites on the surface. To explain the reaction mechanism for CCl2F2 catalytic decomposition over MoO3/ZrO2, a surface intermediate, Osurface-CF2-Osurface is proposed.


2013 ◽  
Vol 726-731 ◽  
pp. 535-538
Author(s):  
Tian Cheng Liu ◽  
Yu Jiao Guo ◽  
Ping Ning ◽  
Guang Yang Tang ◽  
Ming Long Yuan

Catalytic hydrolysis decomposition of dichlorodifluoromethane (CCl2F2) in the presence of water vapor and oxygen was studied over solid acid MoO3/ZrO2 using a fixed-bed reactor. The CCl2F2 adsorption was multilayer chemical adsorption and its process was corresponding with Freundlich model. Its heat was from 56.3 to 73.2 KJ.mol-1, and it was exothermic reaction and chemical adsorption.


2010 ◽  
Vol 150-151 ◽  
pp. 1710-1713
Author(s):  
Ying Jie Zhang ◽  
Yue Xiao Tian ◽  
Da Peng Li ◽  
Guo Rui Liu ◽  
Li Zhang ◽  
...  

A new Fenton-like catalyst was prepared to degrade Orange IV in water by catalytic decomposition of H2O2. The optimal preparation conditions were discussed. The catalytic activity of catalyst was evaluated by the degradation of Orange IV and the decomposition of H2O2. The results show that solid super acid (S2O82-/FexOy) soaked in (NH4)2S2O8 is the most effective catalyst among the synthesized iron oxides soaked in other oxidants. The optimal conditions for solid super acid preparation are calcined at 500 for 2 h in the air.


Author(s):  
Kotaro Nakamura ◽  
Masashi Tanabe ◽  
Satoru Abe ◽  
Takashi Mawatari ◽  
Takao Nakagaki

Abstract At the Fukushima Daiichi nuclear power plant, zirconium in the fuel rod cladding reacted with water vapor at elevated temperatures due to a loss of cooling water, resulting in the production of a large amount of hydrogen. This hydrogen leaked from the reactor vessel and accumulated in the top of reactor building, eventually leading to an explosion. A hydrogen treatment system that re-oxidizes hydrogen to water vapor is one of the effective methods to prevent such an explosion. A prominent re-oxidation method is via a fixed bed reactor packed with metal oxide pellets. The advantages of this method are its relatively fast oxidation rate without external oxygen/air injection. In this study, experiments and complementary numerical calculations were performed on the hydrogen re-oxidation reaction by metal oxides. The oxidation of hydrogen by copper oxide is modeled by 5 interacting, elementary reactions consisting of 6 chemical species. Experiments were performed using two packed bed set-ups, with measurement of inlet/outlet gas composition and pre/post-analysis of solid composition used to determine constants of the individual reaction rates for numerical calculations. From these reaction constants, the temporal behavior of the outlet gas was predicted.


2012 ◽  
Vol 549 ◽  
pp. 109-112
Author(s):  
Jia Wei Qu ◽  
Min Wei Wang ◽  
Ren Lang Wang

Different solid base catalysts used for the polymerization of glycerol were prepared by impregnation. Catalyst type and the preparation conditions were optimized on the base of polymerization degree. Results showed: the best catalyst was KF/Al2O3, and optimal condition for catalyst preparation was as follows: loading of 40% KF, calcinations temperature 600°C. The polymerization degree of 5.92 was obtained under the following reaction condition: the amount of catalyst 11.62,reaction temperature 250°C, reaction time 4 h.


2013 ◽  
Vol 781-784 ◽  
pp. 308-311 ◽  
Author(s):  
Xin Li ◽  
Wei Su ◽  
Qi Bin Xia ◽  
Zhi Meng Liu

Manganese and cerium based catalysts with different Mn/Ce molar ratios prepared by impregnation method for ethyl acetate oxidation. The activity tests of the samples were performed in a fixed-bed reactor. The effect of gas hourly space velocity (GHSV) and ethyl acetate concentration on the catalytic activity of the catalyst were also investigated. The results showed that these catalysts had high activity for the catalytic oxidation of ethyl acetate, of which the catalyst Mn0.9Ce0.1Ox/TiO2exhibitedthe bestactivity, and the temperature required for 90% conversion of ethyl acetate was at 216 °C. The catalyst Mn0.9Ce0.1Ox/TiO2still maintained high activity in the range of GHSV (16,500 to 48,500 h-1) and ethyl acetate concentration (4526 to 7092 mg/m3). In additional, experiments for measuring stability of Mn0.9Ce0.1Ox/TiO2were carried out, and experimental results showed that the good stability of Mn0.9Ce0.1Ox/TiO2was kept after it has run for 25 hours.


2015 ◽  
Vol 802 ◽  
pp. 431-436
Author(s):  
Siti Aminah Md Ali ◽  
Ku Halim Ku Hamid ◽  
Kamariah Noor Ismail

Five series of silica supported bimetallic oxide (NiCo/SiO2) catalysts have been synthesized through successive reverse co-precipitation and wet impregnation methods at different metal loadings (i.e. 80Ni20Co/SiO2,, 60Ni40Co/SiO2,50Ni50Co/SiO2,40Ni60Co/SiO2,20Ni80Co/SiO2). The catalytic performance of these catalysts were tested for the CO2methanation catalysis using microactivity fixed bed reactor. Nickel rich catalyst (80Ni20Co/SiO2) exhibited the highest catalytic activity in the CO2methanation with 47.1% of CO2conversion. Meanwhile, the CH4selectivity and yield was found to be at 99.9% and 27%, respectively.


Sign in / Sign up

Export Citation Format

Share Document