Electrophilic ethylation and nitration of Illinois No. 6 coal was carried out using CH3CH2F:SbF, in SOZ at -40°C and NO,+ BFq in trimethylphosphate solution at room temperature, respectively. The effect of these substituents on the reactivity of coal under the HF:BF,:H, coal liquefaction system was
Superacid coal chemistry. 2. Model compound studies under conditions of HF:BF3:H2 catalysed mild coal liquefaction
✍ Scribed by George A. Olah; Altaf Husain
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 582 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0016-2361
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✦ Synopsis
Selected model compounds representing coal structural entities were studied under the conditions of HF-BF,H, catalysed mild coal liquefaction. Bibenzyl and diphenylmethane gave near quantitative conversion at room temperature without added hydrogen. Biphenyl, however, required hydrogen pressure at 150°C and gave a conversion of only 230%. Among the model compounds containing ether linkages, dibenzyl ether and benzyl phenyl ether gave quantitative conversion at room temperature without added hydrogen. Diphenyl ether in contrast was converted (~70% yield) only under hydrogen pressure at 155°C. Sulphur-and nitrogen-containing model compounds were also studied. At 95°C in the absence of hydrogen, benzyl phenyl sulphide and dibenzyl sulphide gave over 95% conversion. On the other hand diphenyl sulphide and diphenyl disulphide required hydrogen pressure at 150°C to give conversions of z95%. Quinoline gave a conversion of 220% under hydrogen pressure at 15uC. The formation of condensation products in these conversion processes could be suppressed by the use of a good hydrogen donor, such as isopentane.
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