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Hydrogen Sorption In Transition Metal Modified Ets-10

机译:过渡金属修饰的Ets-10中的氢吸附

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摘要

Hydrogen adsorption studies in nickel, rhodium and palladium exchanged and in situ loaded titanosilicate ETS-10 were performed at 77.4 K using a static volumetric adsorption system up to 1 bar, and 303 K in a gravimetric adsorption system up to 5 bar. The hydrogen adsorption isotherms at 77.4 K were reversible with pressure but chemisorption of hydrogen was noticed at 303 K. Rhodium exchanged ETS-10 showed the highest hydrogen adsorption capacity of 82.6 cc/g at 77.4 K. The hydrogen adsorption isotherm analysis at 303 K was repeated up to three adsorption runs to check the repeatability of hydrogen uptake. At 303 K palladium loaded ETS-10 showed the highest hydrogen uptake capacity of 33.1 cc/g. The DRIFT spectra analysis of ETS-10 samples before and after hydrogen adsorption was conducted, which confirmed that the hydrogen adsorbed in transition metal modified ETS-10 at 303 K was due to the chemical interactions in the form of transition metal hydrides inside ETS-10. The absorbed hydrogen at 303 K can be desorbed by heating the ETS-10 sample up to 413 K.
机译:在交换容量为7 bar的镍,铑和钯以及原位负载的钛硅酸盐ETS-10中,氢的吸附研究是使用静态体积吸附系统(最大压力为1 bar)和303 K在重量分析吸附系统(最大压力为5 bar)下进行的。在77.4 K的压力下氢吸附等温线是可逆的,但在303 K时发现氢的化学吸附。铑交换的ETS-10在77.4 K时显示出最高的氢吸附容量82.6 cc / g。在303 K时的氢吸附等温线分析为重复进行多达三个吸附运行,以检查氢吸收的可重复性。 303 K负载钯的ETS-10的最高氢吸收容量为33.1 cc / g。对ETS-10样品进行氢吸附前后的DRIFT光谱分析,证实了在303 K下吸附在过渡金属改性的ETS-10中的氢是由于ETS-10内部以过渡金属氢化物形式发生的化学相互作用。可以通过将ETS-10样品加热到413 K来解吸在303 K处吸收的氢。

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