Maximizing the number of oxygen-containing functional groups on activated carbon by using ammonium persulfate and improving the temperature-programmed desorption characterization of carbon surface chemistry

Carbon ◽  
2011 ◽  
Vol 49 (15) ◽  
pp. 5002-5013 ◽  
Author(s):  
Na Li ◽  
Xiaoliang Ma ◽  
Qingfang Zha ◽  
Kyungsoo Kim ◽  
Yongsheng Chen ◽  
...  
1971 ◽  
Vol 44 (2) ◽  
pp. 307-343 ◽  
Author(s):  
Donald Rivin

Abstract Carbon surface chemistry is relatively new as an independent subject of inquiry, and, judging by the volume of publications, is receiving increasing attention throughout the world. Our conception of carbon black and its functional behavior has changed significantly since the pioneering publication by Studebaker in 1957. Within the last few years there have been a number of excellent reviews covering various aspects of carbon chemistry by authors who are presently active in this field. Donnet, Puri, and Boehm discuss reactions of carbon and the characterization of surface functional groups while van der Plas is particularly thorough on the subject of adsorption properties and porosity. Deviney explores the relationship between surface chemistry and carbon-elastomer interactions, as does Studebaker from the point of view of the practical application of carbon black in rubber. Current monographs containing useful background information are collected in “Les Carbones” and in Walker's continuing series, “Chemistry and Physics of Carbon”. This review will describe how information from diverse sources has contributed to our understanding of the surface reactivity and fundamental adsorption behavior of carbon. It will be shown that most properties of carbon blacks are consistent with a surface structure wherein large deformed basal layers conforming to the topography of the surface are composed of several planar aromatic domains with functional groups at edge and defect sites. Examples of strong molecular interactions are given which involve specific reaction with the basal surface, individual functional groups, or a combination of both.


Carbon ◽  
2008 ◽  
Vol 46 (12) ◽  
pp. 1544-1555 ◽  
Author(s):  
Honória F. Gorgulho ◽  
João P. Mesquita ◽  
Filomena Gonçalves ◽  
Manuel Fernando R. Pereira ◽  
José L. Figueiredo

Catalysts ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 807
Author(s):  
Zen Maeno ◽  
Xiaopeng Wu ◽  
Shunsaku Yasumura ◽  
Takashi Toyao ◽  
Yasuharu Kanda ◽  
...  

In this study, the characterization of In-exchanged CHA zeolite (In-CHA (SiO2/Al2O3 = 22.3)) was conducted by in-situ X-ray diffraction (XRD) and ammonia temperature-programmed desorption (NH3-TPD). We also prepared other In-exchanged zeolites with different zeolite structures (In-MFI (SiO2/Al2O3 = 22.3), In-MOR (SiO2/Al2O3 = 20), and In-BEA (SiO2/Al2O3 = 25)) and different SiO2/Al2O3 ratios (In-CHA(Al-rich) (SiO2/Al2O3 = 13.7)). Their catalytic activities in nonoxidative ethane dehydrogenation were compared. Among the tested catalysts, In-CHA(Al-rich) provided the highest conversion. From kinetic experiments and in-situ Fourier transform infrared (FTIR) spectroscopy, [InH2]+ ions are formed regardless of SiO2/Al2O3 ratio, serving as the active sites.


1995 ◽  
Vol 265 ◽  
pp. 103-110 ◽  
Author(s):  
J.M. Campelo ◽  
A. Garcia ◽  
D. Luna ◽  
J.M. Marinas ◽  
A.A. Romero

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