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首页> 外文期刊>Journal of Membrane Science >High pressure hydrogen permeance of porous stainless steel coated with a thin palladium film via electroless plating
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High pressure hydrogen permeance of porous stainless steel coated with a thin palladium film via electroless plating

机译:通过化学镀钯薄膜涂覆的多孔不锈钢的高压氢渗透率

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摘要

The high-pressure (100-2800 kPa) hydrogen permeance of two membranes, each composed of a thin palladium film (similar to22 mum) deposited on the oxidized surface of a porous stainless steel tubular substrate (0.2 mum grade support) has been determined over the 623-723 K temperature range. The hydrogen flux was proportional to the H-2 partial pressure in the retentate raised to an exponent of similar to0.55 for one membrane and similar to0.64 for the other, indicating that the transport of hydrogen through the composite membrane was primarily limited by bulk diffusion. Overall, the hydrogen permeance of these membranes was within a wide range of values previously reported with thin film palladium membranes of comparable thickness. The first membrane exhibited no detectable helium flux at hydrogen partial pressures less than 350 kPa for a retentate stream composed of 90% hydrogen and 10% helium. H-2/He selectivity decreased to values as low as 12, however, at total transmembrane pressure differentials as great as 2800 kPa. As the membranes were heated from 623 to 723 K under pressures of up to 2800 kPa, the permeance of each membrane remained invariant at values of similar to1.5 x 10(-4) and similar to2.9 x 10(-4) mol/(m(2) s Pa-0.5), then decreased by similar to35% when the membrane was cooled back to 623 K, indicating some degradation of the membranes under the high-pressure testing conditions. Scanning electron microscopy (SEM) analysis revealed that extremes in the palladium film thickness ranged from about 10-50 mum with palladium "fingers" extending into the pore structure anchoring the palladium layer to the support. Although surface characterization could not pinpoint the source of the degradation, intermetallic, diffusion could not be ruled out in spite of the presence of the oxide layer. (C) 2004 Elsevier B.V. All rights reserved.
机译:已经确定了两个膜的高压(100-2800 kPa)氢渗透率,每个膜由沉积在多孔不锈钢管状基材(0.2微米级支撑物)氧化表面上的薄钯膜(类似于22微米)组成。 623-723 K温度范围。氢通量与截留物中的H-2分压成正比,对于一个膜而言,其氢指数升高至类似于0.55的指数,而对于另一种膜而言,则上升至0.64的指数,这表明氢通过复合膜的传输主要受以下因素限制:大量扩散。总的来说,这些膜的氢渗透率在以前报道的具有可比较厚度的薄膜钯膜的宽范围内。对于由90%的氢气和10%的氦组成的截留物流,第一膜在小于350 kPa的氢气分压下未显示出可检测到的氦通量。 H-2 / He选择性降低至低至12的值,但是在跨膜总压差高达2800 kPa时。当膜在高达2800 kPa的压力下从623 K加热到723 K时,每个膜的磁导率保持不变,其值类似于1.5 x 10(-4)mol和2.9 x 10(-4)mol /(m(2)s Pa-0.5),然后在将膜冷却回623 K时降低约35%,表明在高压测试条件下膜会发生一定程度的降解。扫描电子显微镜(SEM)分析表明,钯膜厚度的极限范围为约10-50μm,其中钯“指状物”延伸到将钯层锚定到载体上的孔结构中。尽管表面特征无法确定降解的​​来源,但尽管存在氧化物层,也不能排除金属间的扩散。 (C)2004 Elsevier B.V.保留所有权利。

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