The aluminum chloride catalyzed carbonization of heterocyclic nitrogen compounds such as carbazole, phenazine, and acridine was studied from the viewpoint of the kinetics and the structure of intermediates, in order to elucidate how the similar nitrogen compounds were carbonized to cokes of differen
Carbonization of pitches—IV: Carbonization of polycyclic aromatic hydrocarbons under the presence of aluminum chloride catalyst
✍ Scribed by Isao Mochida; Keiko Kudo; Noriyoshi Fukuda; Kenjiro Takeshita; Ryohei Takahashi
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 831 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0008-6223
No coin nor oath required. For personal study only.
✦ Synopsis
Using aluminum chloride as a catalyst, polycyclic aromatic hydrocarbons were converted into carbons of two different structures, although at the early stage all carbonization processes proceeded via molten phase. The structures were examined with an optieal microscope under crossed nicols. The firs1 type of structure was a flow pattern with large oriented needle like domains observed for carbons obtained from naphthalene, chrysene, and anthracene, whereas the second one was a mosaic structure for carbon from pyrene. A significant subsequent graphitization at 2500°C (as expressed by L, ) took place for both types regardless of the different size of oriented domains. The orientation of domains depends on the rate of carbonization controlled by the holding temperature, time and quantity of the catalyst. Appropriate conditions of carbonization suppressing too fast generation of nuclei so as to permit the formation of ordered arrangement of condensed molecules were found to yield a needle-like coke also from pyrene, thus showing that the passing through a molten phase is not a sufficient condition for formation of a needle-like structure.
📜 SIMILAR VOLUMES
Microscopic observation of carbons obtained from pure aromatic hydrocarbons by the aid of carbonization catalysts was carried out to clarify the microstructure of these carbons of different features. Reflected polarized-light microscopy distinguished needle, mosaic and isotropic cokes, former two of
## Abstract The reaction of __o__‐phthalaldehyde with several aromatic nitro compounds in the presence of carbon monoxide and catalytic quantities of hexarhodium‐hexadecacarbonyl eventuated in the formation of the corresponding N‐substituted isoindolinone as the major product. A reaction mechanism