A well-defined modification of poly(tetrahydr0furan)s was realized by grafting with maleic anhydride. The grafted products were investigated by Fourier-transform infrared (FTIR) spectroscopy and l3C nuclear magnetic resonance (NMR) spectroscopy. FTIR spectroscopy evidenced a characteristic shift of
Cationic grafting of poly(tetrahydrofuran) onto the surface of carbon black
โ Scribed by Norio Tsubokawa; Naoki Takeda; Akira Kanamaru
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- English
- Weight
- 179 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0008-6223
No coin nor oath required. For personal study only.
โฆ Synopsis
Letters to the Editor for cylindrical pores, that is area = (4) (volume in large P. L. WALKER, JR. pores)/(&). This is expected following the disappearance of the A. OYA open super micropores. 0. P. MAHAIAN
This study thus shows that great flexibility exists in the preparation of glassy carbons as catalyst supports. If desired, samples can be prepared which have a system of large pores superimposed on an open super micropore system. On the other hand, samples can also be prepared which only have an open system of large pores. The choice of support will depend upon the size of the reactant and product molecules for the reaction to be catalyzed. If the reaction involves large molecules, such as in the hydrodesulfurization of heavy oils or liquefaction of coal, a glassy carbon having pores of only a large size will be chosen. If on the other hand, a selective catalysis reaction is of interest, such as selective hydrogenation of CO to low molecular weight organics, the presence of a super micropore system will be necessary.
๐ SIMILAR VOLUMES
## Abstract The hydroxy methyl groups were introduced onto the pristine carbon black surface through the reaction between unsaturated hydrogen atoms of the polycondensed aromatic rings of carbon black and formaldehyde in alkali condition. Using the resultant hydroxy methyl groups on the carbon blac
The grafting of polymers onto a carbon black surface based on the trapping of polymer radicals by polycondensed aromatic rings of the surface was investigated. It was found that polymer radicals formed by the thermal decomposition of azo-polymer, peroxy-polymer and 2,2,6,6-tetramethylpiperidinyl-1-o