Study of ion/molecule reactions of ion derived from tert-butyl methyl ether and trimethylsilyl methyl ether
✍ Scribed by Michael Büchner; Hans Friedrich Grützmacher
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 284 KB
- Volume
- 199
- Category
- Article
- ISSN
- 1387-3806
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Synthesis of methyl tert-butyl ether (abbreviated as MTBE) from methanol (MeOH) and tert-butyl alcohol (TBA) in the liquid phase was studied by using Amberlyst 15 in the Hi form as an acid catalyst. Experiments were carried out in a stirred batch reactor at different temperatures (313, 318, and 323
UV spectra and kinetics for the reactions of alkyl and alkylperoxy radicals from methyl tert-butyl ether (MTBE) were studied in 1 atm of SF, by the pulse radiolysis-UV absorption technique. UV spectra for the radical mixtures were quantified from 215 to 340 nm. At 240 nm, a, = (2.6 f 0.4) X lo-l8 cm
## Abstract The process can yield methyl esters or a mixture of tert‐butyl and methyl esters depending on the temperature.
Synthesis of tert-amyl methyl ether (TAME) from methanol (MeOH) and tert-amyl alcohol (TAA) in the liquid phase was studied by using an ion exchange resin, Amberlyst15 (A15) in the H ϩ form. Experiments were carried out in a stirred batch reactor under atmospheric pressure. The effects of catalyst s