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Fischer Tropsch Synthesis in Supercritical CO_2

机译:Fischer托幼船在超临界CO_2中的合成

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The results from studies on Fischer Tropsch synthesis wherein syngas was dissolved in CO_2 are presented. In addition CO_2 reduction by hydrogen under these conditions were also analyzed. It was found that the CO_2 behaves both a s a solven/diluent as well as a reactant. The syngas used was typical of that obtained from coal gasification, i.e. CO:H_2 of one. Under these conditions Co-based catalysts without any water gas shift catalyst does not perform well while Fe - based catalysts have been found to be useful. However, the Fe based catalysts have a propensity towards CO_2 selectivity via the primary FT reaction, Boudouard reaction and the water gas shift reaction. The use of CO_2 as a solvent was found to suppress the CO_2 and CH_4 selectivity while enhancing the hydrocarbon selectivity and CO conversion when FT synthesis was conducted using coal derived syngas on Fe-Zn-K catalysts. The effects were found to be significantly pronounced at pressures higher than or equal to 1200 psi. It should be noted that CO_2 is supercritical at pressures higher than 1050 psi and 31.4 °C. The effect of CO_2 partial pressure, reactor pressure, reaction temperature, catalyst loading and H_2:CO ratio in syngas on the liquid product distribution will be presented. Some of the notable findings include negative CO_2 selectivities while obtaining nearly 98% CO conversion. Increasing the reactor pressure was found to favor longer chain growth. In addition, it is noted that the ratio between CO_2:syngas in the reaction mixture is an important factor in the liquid product distribution. A higher value of the ratio is seen to favor hydrocarbon synthesis, while a lower value of the ratio favors oxygenate production particularly pentanols and butanols. In addition, the data on the once through fractionation of the products utilizing the solubilities in supercritical CO_2 and pressure tuning will be presented. It will be shown that the products can be easily fractionated into narrow carbon chain length distributions downstream of the reactor by simply reducing the pressures in each collection vessel. It was generally observed that the oxygenates and higher n-alkanes were collected in the higher pressure trap and lower hydrocarbons in the subsequent lower pressure traps. Residence time studies were conducted and the effect of conversion and reaction rates on the residence time and feed composition were evaluated. Long term catalyst life studies were conducted and it was found that the use of supercritical CO_2 enhanced the life of the catalyst as opposed to pure syngas feed. This research was made possible with support, in part, by the Illinois Department of Commerce and Economic Opportunity through the Office of Coal Development and the Illinois Clean Coal Institute and the Office of Vice Chancellor for Research at Southern Illinois University, Carbondale.
机译:提出了对Fischer Tropsch合成的研究结果,其中将合成气溶解在CO_2中。此外,还分析了在这些条件下通过氢的CO_2减少。发现CO_2表现为S溶剂/稀释剂以及反应物。所使用的合成气是典型的,即从煤气化获得,即一个:h_2。在这些条件下,没有任何水煤气变换催化剂的基型催化剂在发现Fe基催化剂是有用的同时不能很好地表现良好。然而,Fe基催化剂通过初级FT反应,Boudouard反应和水煤气变换反应对CO_2选择性具有倾向倾向。发现使用CO_2作为溶剂抑制CO_2和CH_4选择性,同时使用Fe-Zn-K催化剂上的煤衍生的合成法进行FT合成时增强烃选择性和CO转化。发现效果在高于或等于1200 psi的压力下显着明显明显。应该注意的是,CO_2在高于1050 psi和31.4°C的压力下超临界。将介绍CO_2分压,反应器压力,反应温度,催化剂负载和H_2:合成气中的液体产物分布中的共比的影响。一些显着的发现包括负CO_2选择性,同时获得近98%的CO转化。发现增加反应器压力有利于更长的链生长。另外,注意到反应混合物中CO_2:合成气之间的比例是液体产物分布的重要因素。观察到较高的比例值以有利于烃合成,而该比率的较低值尤其是碳酸盐产生特别是戊醇和丁醇。此外,还将介绍一下,通过利用超临界CO_2和压力调整中的溶解度进行一次通过分馏的数据。将表明,通过简单地减少每个收集容器中的压力,可以容易地分馏在反应器下游的窄碳链长度分布中。通常观察到,在随后的低压陷阱中,在较高的压力阱和低级烃中收集含氧化合物和更高的N-烷烃。进行了停留时间研究,评估了转化率和反应速率对停留时间和饲料组合物的影响。进行了长期催化剂寿命研究,发现超临界CO_2的使用增强了催化剂的寿命,而不是纯合成气饲料。通过煤炭发展办公室和伊利诺伊州清洁煤炭研究所和南伊利诺伊州南部大学研究所,伊利诺伊州的商业和经济机会,伊利诺伊商务部和经济机会,这项研究是可能的。

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