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Development and testing of a combined catalyst/sorbent core-in-shell material for the production of high concentration hydrogen.

机译:开发和测试用于生产高浓度氢气的组合催化剂/吸附剂核壳材料。

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A combined catalyst and sorbent for the production of hydrogen from CH 4 or CO was developed and tested. The combined catalyst and sorbent was a spherical multi-layered material having a CaO-based sorbent core and an outer shell composed mainly of alumina. The CaO sorbent core was employed to absorb CO2, one of the reaction products. The alumina shell protected the friable CaO core and also supported a Ni catalyst. The development of the material focused separately on the development of the core and shell. First, since the CO2 absorption capacity of CaO-based sorbents diminishes as they are repeatedly used and regenerated, the development of a more stable CaO-based sorbent was investigated. Both the addition of MgO, which acted as a sintering inhibitor, and severe initial calcination conditions for the CaO precursor limestone produced a more stable CaO sorbent. Second, an alumina-based material with good physical strength and high surface area was developed to serve as the shell of the core-in-shell material. The addition of either fine particle limestone or lanthanum oxide to the alumina shell formulation produced a material with enhanced physical strength, which was most likely due to the formation of a binding aluminate phase.;Reaction testing of the core-in-shell pellets with a 3:1 molar ratio of H2O:CH4 in the feed produced a high concentration of H2 via simultaneous application of the steam-methane reforming reaction, the water-gas shift reaction and the reaction of CO2 with CaO. This testing was conducted with a tubular fixed bed reactor over a temperature range of 550-650°C and a pressure range of 1.0-10.0 atm. The rapid absorption of CO2 by CaO produced CH4 and CO conversions greater than would have been possible without a sorbent. Lifecycle testing determined that a high concentration of H2 could be produced over 10 cycles of H2 production and sorbent regeneration. However, the length of time that H2 was produced diminished with each cycle due to a loss of CO2 absorption capacity by the CaO sorbent. Physical characterization of the pellets after lifecycle testing also revealed that some pellets fractured during lifecycle testing and that the Ni catalyst sintered.;Core-in-shell pellets with alternate shell formulations were also tested in the fixed bed reactor for the production of high concentrations of H 2 from a mixture of CO and steam via the water-gas shift reaction. Three alumina shell formulations were tested: a formulation with mostly alumina in the shell, a formulation with 10 wt% Fe2O3 added to the alumina shell formulation and a formulation with Ni impregnated onto the shell. The rapid absorption of CO2 by the sorbent allowed for a high concentration of H2 to be produced and a high CO conversion to be achieved between 550-600°C at 1.0 atm with any of these formulations. However, once the CaO sorbent became loaded, only the formulation with Ni present converted CO to reaction equilibrium levels. On the other hand, by absorbing CO2 the formulation with mainly alumina in the shell appeared to be an attractive material for the production of H 2 from syngas. Furthermore, this formulation would be resistant to sulfurous gases that might be present.
机译:开发并测试了用于从CH 4或CO生成氢的催化剂和吸附剂的组合。组合的催化剂和吸附剂是具有CaO基吸附剂芯和主要由氧化铝组成的外壳的球形多层材料。 CaO吸附剂芯用于吸收反应产物之一的CO2。氧化铝壳保护了易碎的CaO核,还负载了Ni催化剂。材料的开发分别集中在核和壳的开发上。首先,由于随着重复使用和再生CaO基吸附剂的CO 2吸收能力下降,因此研究了更稳定的CaO基吸附剂的开发。用作烧结抑制剂的MgO的添加以及CaO前体石灰石的严格初始煅烧条件都产生了更稳定的CaO吸附剂。其次,开发了具有良好的物理强度和高表面积的氧化铝基材料以用作核壳材料。在氧化铝壳配方中添加细颗粒石灰石或氧化镧可产生具有增强的物理强度的材料,这很可能是由于铝酸盐粘结相的形成所致。通过同时应用蒸汽-甲烷重整反应,水煤气变换反应和CO2与CaO的反应,进料中H2O:CH4摩尔比为3:1产生高浓度的H2。用管状固定床反应器在550-650℃的温度范围和1.0-10.0atm的压力范围内进行该测试。 CaO对CO2的快速吸收产生的CH4和CO转化率要比没有吸附剂时高。生命周期测试确定,在H2产生和吸附剂再生的10个循环中可以产生高浓度的H2。但是,由于CaO吸附剂会损失CO2吸收能力,因此每个循环产生H2的时间长度都会减少。生命周期测试后对颗粒的物理表征还表明,在生命周期测试中一些颗粒会破裂,并且Ni催化剂会被烧结。在固定床反应器中还测试了具有交替壳配方的核壳颗粒,以生产高浓度的通过水煤气变换反应从CO和蒸汽的混合物中提取H 2。测试了三种氧化铝壳配方:壳中主要含氧化铝的配方,向氧化铝壳配方中添加10 wt%Fe2O3的配方以及在壳中浸渍了Ni的配方。这些配方中的任何一种均可通过吸附剂快速吸收CO2,从而产生高浓度的H2,并在550-600°C和1.0atm的温度下实现高CO转化率。但是,一旦负载了CaO吸附剂,只有含Ni的配方才会将CO转化为反应平衡水平。另一方面,通过吸收CO 2,壳中主要是氧化铝的制剂似乎是从合成气生产H 2的有吸引力的材料。此外,该制剂将抵抗可能存在的亚硫气体。

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