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重整氣中CO深度去除方法

Deep removal of CO in reformate

  • 摘要: 提出了兩段CO深度去除法(M-O法):第1段采用選擇性甲烷化和第2段采用選擇性氧化,即對水汽變換(WGS)反應器出口約含體積分數為1%CO的重整氣進行選擇性甲烷化,將CO去除至0.1%以下,而后進行選擇性氧化將CO去除至10×10-6以下.實驗結果表明:一方面,與兩段選擇性甲烷化CO深度去除法(M-M法)相比,M-O法具有相近的熱效率,工作溫度移向低溫,可在更寬的溫度區間和更高的空速下滿足CO去除深度的要求;另一方面,M-M法系統簡單,而M-O法具有反應器更加緊湊的優勢.此外,還探討了在上述兩種工藝過程的后段再附加上一段高空速選擇性氧化過程,可將CO的去除深度進而提高到1×10-6以下,更加有利于質子交換膜燃料電池電站系統長時間連續運行的穩定性.

     

    Abstract: CO deep removal was investigated by combining preferential methanation and preferential oxidation(M-O method).In the M-O method,CO of about 1% in reformate from a water gas shift(WGS) reactor is reduced to about 0.1% in the first stage of preferential methanation,then further reduced to below 10×10-6 in the second stage of preferential oxidation.The results show that in comparison of the M-M method(a method of CO deep removal with two-stage preferential methanation) the M-O method could be operated with a wider temperature range and a higher gas hourly space velocity at a lower temperature,and has almost the same thermal efficiency.In the other hand,although a reaction system of the M-M method is simpler,a reaction reactor of the M-O method could be more compact in comparison.In addition,a high-speed preferential oxidation step set at the outlet of the second stage in the M-M method or M-O method was proposed to remove CO to below 1×10-6,which helps to enhance the stability of proton exchange membrane fuel cells under long time continuous running.

     

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