Related Experiment Video
Updated: Sep 16, 2025

Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating
Published on: December 25, 2016
Study on the Surface Functional Groups of Asphaltenes Pre- and Post-Hydrotreating in Different Reaction Systems
Yudong Sun1, Zezhou Wang2, Ziyuan Liu1
1College of Chemistry & Chemical Engineering, China University of Petroleum(East China), Qingdao 266580, China.
None:
The surface functional groups of asphaltenes pre- and post-hydrotreating in different reaction systems were investigated by X-ray photoelectron spectroscopy (XPS). The asphaltenes were separated by different solvents from the Yumen atmospheric residue (YMAR) and the Merey atmospheric residue (MRAR) pre- and post-hydrotreating in the residue and decalin. The results show that asphaltene is mainly composed of carbon, sulfur, nitrogen, and oxygen in addition to hydrogen. The carbon atoms exist in the forms of sp2 and sp3, but there are fewer carbon atoms combined with oxygen atoms in asphaltene. Oxygen mainly exists in the forms of ketonic oxygen, carbon-oxygen single bond, and carboxyl oxygen in asphaltene. The carbon-oxygen single bond is the main existing form of oxygen, and the ketonic oxygen decreases in hydrotreated asphaltene. The nitrogen is mainly pyrrole nitrogen in asphaltene, the pyrrole nitrogen further increases, and the pyridine nitrogen is reduced to less than one-third after hydrotreating. Alkyl sulfur is higher than thiophene sulfur in proto-asphaltene. Although the content of thiophene sulfur is increased in hydrotreated asphaltene, alkyl sulfur still dominates.
More Related Videos
12:08Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
06:31Studying Surfactant Effects on Hydrate Crystallization at Oil-Water Interfaces Using a Low-Cost Integrated Modular Peltier Device
Published on: March 18, 2020
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Introduction to Functional Groups
Functional groups are group of atoms with specific chemical properties that occur within organic molecules and sometimes denoted as “R”. Functional groups are found along the carbon backbone of macromolecules can form chains or rings of carbon atoms. Functional groups can “functionalize” a compound by enabling it to adopt different physical and chemical properties.
Types of common functional groups
The table below summarizes some of the major functional...
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Acetals and Thioacetals as Protecting Groups for Aldehydes and Ketones
In the presence of multiple functional groups, when selective reduction of one group over the other is desired, groups like aldehydes and ketones that form acetals...