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DENSE MEMBRANES FOR SEPARATION OF H_2 FROM CO_2 IN HIGH-PRESSURE WATER-GAS SHIFT REACTORS

机译:用于在高压水 - 气体换料反应器中从CO_2分离H_2的致密膜

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Studies were performed to determine the feasibility of using various dense hydrogen transport membranes for economical separation of hydrogen from CO_2 in high-pressure water-gas shift reactors. As an alternative to burning fuels directly in air, all carbonaceous materials, in principle, can be steam reformed into a mixture of H_2 + CO. The CO can be further reacted with steam in water-gas shift reactors operating above 30 bar and 340-440EC to form CO_2 and additional H_2. If membranes were commercially available to separate CO_2 from H_2 in water-gas shift reactors, the hydrogen could be utilized as a clean fuel, and the CO_2, remaining at high pressure and undiluted by nitrogen, would be in a very concentrated form desirable for economic sequestration. Dense membranes have an advantage over porous membranes in that they possess essentially 100% selectivity for hydrogen. Proton conducting ceramic membranes, thin palladium membranes supported on porous ceramic substrates, cermet membranes, and dense metallic membranes were all investigated in this program. Membranes made from metals and alloys of Group ⅣB and ⅤB elements (i.e. Nb, Ta, V, Zr) exhibited the best overall performance. These materials have long been used as hydrogen separation membranes in the nuclear industry and possess hydrogen permeabilities 10 to 100 times better than palladium in the desired temperature range of 340-440°C. Preliminary investigations showed that some of these metals were susceptible to hydrogen embrittlement at water-gas shift reactor temperatures and desired partial pressures of hydrogen of up to 13.1 bar. However, select Group IVB and VB metals and their alloys, when utilized appropriately, were capable of record hydrogen flux, at essentially 100% selectivity. Free-standing, unsupported metal disks, 16 mm in diameter, were found to resist a target differential pressure of 31 bar with a partial pressure of hydrogen in the feed of 13.1 bar, while yielding a hydrogen flux of 280 mL min~(-1) cm~(-2) (STP) (2.1 mol m~(-2) s~(-1)) at 440°C. Under an ideal hydrogen/helium atmosphere at 34 bar partial pressure of hydrogen in the feed and 33 bar differential pressure, a record flux of 423 mL min~(-1) cm~(-2) (STP) (3.1 mol m~(-2) s~(-1)) at 440°C was achieved. It was concluded that the all-metal membranes appear superior for separation of H_2 from CO_2 and steam at high pressure.
机译:进行研究以确定使用各种致密氢输送膜的可行性,以便在高压水 - 气体移位反应器中从CO_2经济分离氢气。作为直接在空气中燃烧燃料的替代方案,原则上,所有碳质材料都可以将蒸汽重整成H_2 + CO的混合物。该CO可以进一步反应在30巴以上工作的水 - 气体移位反应器中的蒸汽和340- 440EC形成CO_2和额外的H_2。如果膜可商购获得从水 - 气体换体反应器中的H_2分离CO_2,则氢可以用作清洁燃料,并且CO_2保持高压并受氮的未稀释,将以非常浓缩的形式以经济为理想的形式封存。致密膜具有多孔膜的优点,因为它们具有基本上100%的氢选择性。在该计划中,全部研究了质子传导陶瓷膜,负载在多孔陶瓷基材,金属陶瓷膜和致密金属膜上的薄钯膜。由B和B元素的金属和合金制成的膜(即Nb,Ta,V,Zr)表现出最佳的整体性能。这些材料长期被用作核工业中的氢分离膜,并且在340-440℃的所需温度范围内具有比钯更好的氢渗透率10至100倍。初步研究表明,一些这些金属在水 - 气体移位反应器温度下易受氢气脆化的影响,以及最多13.1巴的氢的所需部分压力。然而,选择基团IVB和VB金属及其合金,当适当地使用时能够记录氢气通量,基本上100%选择性。发现独立式的无支撑的金属磁盘,直径为16毫米,抵抗31巴的目标差压,其中氢气的部分压力为13.1巴,同时产生280mL min〜(-1)的氢通量〜(-1 )Cm〜(-2)(STP)(2.1mol m〜(-2)s〜(-1)),440℃。在进料和33巴差压的34巴氢/氦气氛下在34巴的部分压力下,423ml min〜(-1)cm〜(stp)的记录通量(3.1mol m〜( -2)达到440°C的S〜(-1))。得出结论是,全金属膜显得优于H_2在高压下从CO_2和蒸汽分离。

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