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首页> 外文期刊>Thermochimica Acta: An International Journal Concerned with the Broader Aspects of Thermochemistry and Its Applications to Chemical Problems >Thermogravimetric determination of coke deposits on alumina-supported noble metal catalysts used as hydrodechlorination catalysts
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Thermogravimetric determination of coke deposits on alumina-supported noble metal catalysts used as hydrodechlorination catalysts

机译:热重法测定用作加氢脱氯催化剂的氧化铝负载贵金属催化剂上的焦炭沉积

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摘要

The deactivation of 0.5 wt.% Pd on alumina, 0.5 wt.% Rh on alumina and 0.5 wt.% Pt on alumina catalysts for the hydrodechlorination of tetrachloroethylene (TTCE) in organic matrix has been studied. Experiments were carried out in a continuous fixed-bed reactor at 250 degreesC, 5 bar, 1.3 g catalyst min/mmol TTCE and 0.8 nl/min of hydrogen. The Pd catalyst is the most stable at the studied conditions, followed by Rh and Pt. In order to study the causes of deactivation, fresh and used catalysts were characterised by nitrogen porosimetry, X-ray diffraction (XRD), thermogravimetry (TG), X-ray photoelectron spectroscopy (XPS), temperature-programmed oxidation (TPO) and pulse hydrogen chemisorption. Characterisation results indicate that the deactivation is caused mainly by the formation of carbonaceous deposits, being negligible the effects of poisoning by HCL It was observed that in addition to the amount of coke, its combustion temperature is an important parameter, showing a higher capacity to deactivate the catalysts the cokes with lower combustion temperatures (obtained from differential thermogravimetry (DTG) profiles). (C) 2001 Elsevier Science B.V. All rights reserved. [References: 14]
机译:对于有机基质中四氯乙烯(TTCE)的加氢脱氯,已经研究了氧化铝上0.5 wt。%Pd,氧化铝上0.5 wt。%Rh和氧化铝上0.5 wt。%Pt的失活。在连续固定床反应器中于250℃,5 bar,1.3 g催化剂min / mmol TTCE和0.8 nl / min的氢气下进行实验。在研究条件下,Pd催化剂最稳定,其次是Rh和Pt。为了研究失活的原因,通过氮气孔隙率法,X射线衍射(XRD),热重分析(TG),X射线光电子能谱(XPS),程序升温氧化(TPO)和脉冲对新鲜和用过的催化剂进行了表征。氢化学吸附。表征结果表明,失活主要是由碳质沉积物的形成引起的,可以忽略不计HCL的中毒作用。观察到,除焦炭量外,其燃烧温度是重要的参数,显示出更高的失活能力催化剂的焦炭燃烧温度较低(从差示热重分析(DTG)曲线获得)。 (C)2001 Elsevier Science B.V.保留所有权利。 [参考:14]

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