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| 生物质气化尾气CO_2联合微波重整甲苯制备合成气 | |
| 引用本文： | 李龙之,宋占龙,马春元,王孚懋,田原宇.生物质气化尾气CO_2联合微波重整甲苯制备合成气[J].农业工程学报,2014,30(23):268-274. |
| 作者姓名： | 李龙之 宋占龙 马春元 王孚懋 田原宇 |
| 作者单位： | 1. 山东科技大学机械电子工程学院,青岛,266590 2. 山东大学燃煤污染物减排国家工程实验室,济南,250061 3. 山东科技大学化学与环境工程学院,青岛,266590 |
| 基金项目： | 山东省优秀中青年科学家科研奖励基金（BS2011NJ010）；山东科技大学人才引进科研启动基金（2013RCJJ018） |
| 摘 要： | 该文以甲苯为焦油模型化合物,利用生物质焦炭诱导其转化合成气,探讨加热方式和通入CO2对甲苯转化的影响。结果表明:同等工况下,微波加热(microwave heating,MH)下甲苯转化率高于常规加热(electrical heating,EH),甲苯转化率最大差值为15.58%。通入CO2可促进甲苯转化,MH和EH下分别在CO2流量为80和40 m L/min达到最高转化率93.73%和82.13%。引入CO2可调控甲苯定向制备合成气,且对生物质焦炭造成碳损耗。损耗碳可转化合成气,且CO2通入量越高,其贡献越大。MH下合成气最大产率为173.66 m L/min,为裂解反应的5.68倍。甲苯裂解率持续降至49.0%,之后趋于稳定。甲苯重整转化率维持较高水平,140 min后开始减弱,同时合成气收率平缓降低。该文研究结果对高效利用焦油和减排CO2有借鉴意义。 |
| 关 键 词： | 微波 重整反应 焦油 合成气 生物质焦炭 |
| 收稿时间： | 2014/6/28 0:00:00 |
| 修稿时间： | 2014/11/1 0:00:00 |
Toluene reforming by carbon dioxide recycled from biomass gasification into syngas production under microwave irradiation |
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| Li Longzhi,Song Zhanlong,Ma Chunyuan,Wang Fumao and Tian Yuanyu.Toluene reforming by carbon dioxide recycled from biomass gasification into syngas production under microwave irradiation[J].Transactions of the Chinese Society of Agricultural Engineering,2014,30(23):268-274. | |
| Authors: | Li Longzhi Song Zhanlong Ma Chunyuan Wang Fumao and Tian Yuanyu |
| Institution: | 1. College of Mechanical and Electronic Engineering, Shandong University of Science and Technology, Qingdao 266590, China,2. National Engineering Laboratory for Coal Combustion Pollutants Reduction, Shandong University, Jinan 250061, China,2. National Engineering Laboratory for Coal Combustion Pollutants Reduction, Shandong University, Jinan 250061, China,1. College of Mechanical and Electronic Engineering, Shandong University of Science and Technology, Qingdao 266590, China and 3. College of Chemical and Environmental Engineering, Shandong University of Science and Technology, Qingdao 266590, China |
| Abstract: | Abstract: The quality of gaseous products can be deteriorated by tar, CO2 and other impurities during the process of biomass gasification. Based on the those impurities analysis, tar conversion by CO2 is performed in this paper. Toluene was chosen as a model compound in this study, and it was used for converting into syngas production over a biomass-derived char. Biomass char is obtained from the pyrolysis of corn straw at a microwave-assisted experimental system. The influences of heating method includes microwave heating (MH) and electrical heating (EH) as well as CO2 flow rate on toluene conversion, syngas yield and carbon loss. The results show that toluene conversion from microwave heating is significantly higher than that from electrical heating under the same circumstances. And it is revealed that a maximum difference of toluene conversion between microwave heating and electrical heating is reached up to 15.58% at CO2 flow rate of 80 mL/min. When a certain amount of CO2 is imported, toluene conversion can be improved effectively. The highest toluene conversion of 93.73% is achieved under microwave heating at CO2 flow rate of 80 mL/min, while toluene conversion under electrical heating is reached a peak of 82.13%, corresponding to CO2 flow rate of 40 mL/min. Moreover, the introduction of CO2 can regulate the conversion of toluene into syngas production with a suitable ratio of H2 and CO. At the same time, an excess of CO2 can result in a loss of carbon contained in biomass-derived char. The carbon consumed through the gasification of CO2 can be converted into part of syngas production, which can impose a direct contribution to total syngas yield. With the increase of CO2 flow rate, a higher syngas yield from carbon consumption is achieved. The maximum contribution of carbon consumption to syngas yield is 15.40% under microwave heating at CO2 flow rate of 120 mL/min. According to the results, it is found that the highest yield of syngas derived from toluene reforming by CO2 under microwave heating is 173.66 mL/min when CO2 flow rate is 80 mL/min. And the yield mentioned above is 5.68 times that of syngas obtained from toluene cracking in the absence of CO2. A decrease in the conversion of toluene cracking is revealed, with the advancement of cracking experiment. And continuous decrease in toluene conversion occurred in cracking experiment until the conversion of toluene cracking drops below 49.0%. Afterwards, a stable phase of toluene conversion is seen in toluene cracking. It is fond that the conversion obtained from toluene reforming is maintained at a higher level, compared to that from toluene cracking. After toluene reforming conducted for 140 min, a decrease in toluene conversion is emerged. At the same time, a gentle decrease in the yield of syngas produced from toluene reforming is observed after 140 min. The conclusions of this study have a significant effect on efficient disposal and utilization of tar from biomass gasification. This research can also provide beneficial reference to the emission of CO2. |
| Keywords: | microwaves reforming reactions tar syngas biomass char |
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