High Coke-Resistance Pt/Mg1-xNixO Catalyst for Dry Reforming of Methane

نویسندگان

  • Faris A. J. Al-Doghachi
  • Aminul Islam
  • Zulkarnain Zainal
  • Mohd Izham Saiman
  • Zaidi Embong
  • Yun Hin Taufiq-Yap
  • Gang Yang
چکیده

A highly active and stable nano structured Pt/Mg1-xNixO catalysts was developed by a simple co-precipitation method. The obtained Pt/Mg1-xNixO catalyst exhibited cubic structure nanocatalyst with a size of 50-80 nm and realized CH4 and CO2 conversions as high as 98% at 900°C with excellent stability in the dry reforming of methane. The characterization of catalyst was performed using various kinds of analytical techniques including XRD, BET, XRF, TPR-H2, TGA, TEM, FESEM, FT-IR, and XPS analyses. Characterization of spent catalyst further confirms that Pt/Mg1-xNixO catalyst has high coke-resistance for dry reforming. Thus, the catalyst demonstrated in this study, offers a promising catalyst for resolving the dilemma between dispersion and reducibility of supported metal, as well as activity and stability during high temperature reactions.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Investigation of the catalytic performance and coke formation of nanocrystalline Ni/SrO-Al2O3 catalyst in dry reforming of methane

In this study, nickel catalysts supported on mesoporous nanocrystalline gamma alumina promoted by various strontium contents were prepared by the impregnation method and employed in dry reforming of methane (DRM). The prepared catalysts were characterized using N2 adsorption (BET), temperature-programmed reduction and oxidation (TPR,) and oxidation (TPDTPO), X-ray diffraction (XRD), and scannin...

متن کامل

An Investigation into the Effect of Hydrotalcite Calcination Temperature on the Catalytic Performance of Mesoporous Ni-MgO-Al2O3 Catalyst in the Combined Steam and Dry Reforming of Methane

Several mesoporous nickel-based catalysts with MgO-Al2O3 as the catalyst support were prepared using a co-precipitation method at a constant pH. The supports were prepared from the decomposition of an Mg-Al hydrotalcite-like structure which had already been prepared with Mg/Al=1. Prior to impregnating 10 wt.% nickel on the supports, the precursor was decomposed at several ...

متن کامل

Coke- and sintering-resistant monolithic catalysts derived from in situ supported hydrotalcite-like films on Al wires for dry reforming of methane.

Monolithic catalysts derived from in situ supported hydrotalcite-like films on Al wires display high resistance to coke formation and sintering in the dry reforming of methane due to their hierarchical porous structure, well dispersed metallic nickel species, more basic sites and strong metal-support interaction effect.

متن کامل

Catalytic Reforming of Methane in the Presence of CO2 and H2O at High Pressure

Exploiting the greenhouse gas CO2 as raw material could be more advantageous than its long-term storage. For instance, CO2 can be used on large scale for the production of COrich syngas with a H2/CO ratio of unity. Such a syngas can be used for the synthesis of commodity chemicals like aldehydes and ketones obtained through carbonylation of alkenes in hydroformulation and can be produced by CO2...

متن کامل

CO2 Reforming of Coke Oven Gas Over a Ni/γAl2O3 Catalyst to Produce Syngas for Methanol Synthesis

The CO2 reforming of coke oven gases (COG) was carried out over a Ni/γAl2O3 catalyst in order to obtain a suitable syngas for methanol synthesis. The influence of different operating conditions, such as temperature and volumetric hourly space velocity (VHSV), was studied. It was found that the H2 present in the feed gas promotes the Reverse Water Gas Shift reaction (RWGS), which produces water....

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 11  شماره 

صفحات  -

تاریخ انتشار 2016