A review of catalytic partial oxidation of fossil fuels and biofuels: Recent advances in catalyst development and kinetic modelling

2018 ◽  
Vol 136 ◽  
pp. 385-402 ◽  
Author(s):  
P. Arku ◽  
B. Regmi ◽  
A. Dutta
Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2495
Author(s):  
Daniela Pietrogiacomi ◽  
Maria Cristina Campa ◽  
Ida Pettiti ◽  
Simonetta Tuti ◽  
Giulia Luccisano ◽  
...  

Ni/ZrO2 catalysts, active and selective for the catalytic partial oxidation of methane to syngas (CH4-CPO), were prepared by the dry impregnation of zirconium oxyhydroxide (Zhy) or monoclinic ZrO2 (Zm), calcination at 1173 K and activation by different procedures: oxidation-reduction (ox-red) or direct reduction (red). The characterization included XRD, FESEM, in situ FTIR and Raman spectroscopies, TPR, and specific surface area measurements. Catalytic activity experiments were carried out in a flow apparatus with a mixture of CH4:O2 = 2:1 in a short contact time. Compared to Zm, Zhy favoured the formation of smaller NiO particles, implying a higher number of Ni sites strongly interacting with the support. In all the activated Ni/ZrO2 catalysts, the Ni–ZrO2 interaction was strong enough to limit Ni aggregation during the catalytic runs. The catalytic activity depended on the activation procedures; the ox-red treatment yielded very active and stable catalysts, whereas the red treatment yielded catalysts with oscillating activity, ascribed to the formation of Niδ+ carbide-like species. The results suggested that Ni dispersion was not the main factor affecting the activity, and that active sites for CH4-CPO could be Ni species at the boundary of the metal particles in a specific configuration and nuclearity.


2021 ◽  
Author(s):  
Sai Chen ◽  
Xin Chang ◽  
Guodong Sun ◽  
Tingting Zhang ◽  
Yiyi Xu ◽  
...  

This review describes recent advances in the propane dehydrogenation process in terms of emerging technologies, catalyst development and new chemistry.


Author(s):  
Ying Lin ◽  
Xuesong Li ◽  
Martyn Twigg ◽  
William F Northrop

This work presents a novel non-premixed opposed-flow reactive volatilization reactor that simultaneously vaporizes and partially oxidizes low volatility liquid hydrocarbons at a short contact time (<12 ms). In the reactor,...


Author(s):  
Shuzhuang Sun ◽  
Hongman Sun ◽  
Paul T Williams ◽  
Chunfei Wu

CO2 is one of the most important greenhouse gases leading to severe environmental issues. The increase of CO2 emissions from the consumption of fossil fuels has received much research attention....


Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2539
Author(s):  
Sipei Li ◽  
Yang Liu ◽  
Dana A. Wong ◽  
John Yang

Since the second industrial revolution, the use of fossil fuels has been powering the advance of human society. However, the surge in carbon dioxide (CO2) emissions has raised unsettling concerns about global warming and its consequences. Membrane separation technologies have emerged as one of the major carbon reduction approaches because they are less energy-intensive and more environmentally friendly compared to other separation techniques. Compared to pure polymeric membranes, mixed matrix membranes (MMMs) that encompass both a polymeric matrix and molecular sieving fillers have received tremendous attention, as they have the potential to combine the advantages of both polymers and molecular sieves, while cancelling out each other’s drawbacks. In this review, we will discuss recent advances in the development of MMMs for CO2 separation. We will discuss general mechanisms of CO2 separation in an MMM, and then compare the performances of MMMs that are based on zeolite, MOF, metal oxide nanoparticles and nanocarbons, with an emphasis on the materials’ preparation methods and their chemistries. As the field is advancing fast, we will particularly focus on examples from the last 5 years, in order to provide the most up-to-date overview in this area.


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