Superacids
Mostrando 1-4 de 4 artigos, teses e dissertações.
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1. Comparative study of acid catalysts for biodiesel production / Estudo comparativo de catalisadores ácidos para a produção de biodiesel
Para que o processo de produção de biodiesel se torne auto-sustentado, ou seja, socialmente, ecologicamente e economicamente viáveis, alguns aspectos químicos ainda precisam ser estudados e aprimorados. Dentre estes, dois são relevantes: alta eficiência no rendimento da reação e o uso de catalisadores de maneira ecologicamente responsável. Para aten
Publicado em: 2009
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2. Sintese fotoquimica de polipirrol em membranas microporosas de PVDF : um novo metodo para obter compositos condutores eletricos
This work outlines a new method to obtain conducting composites of Polypyrrole (PPy)/Poly(vinilydene Fluoride) (PVDF), via UV-ligth induced Polymerization in presence of suitable a Photoacid Generator (PAG) compound such as Iron-arene and Triphenyl Sulfonium salts or organic PAG compound such as chlorinated triazines. Gravimetric and Thermal Gravimetric Anal
Publicado em: 1995
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3. Comparison of the nitration of polyfluoronitrobenzenes by nitronium salts in superacidic and aprotic media: activation of the nitronium ion by protosolvation.
The reactivity of nitronium tetrafluoroborate in the nitration of deactivated di- and trifluoronitrobenzenes is enhanced in superacidic trifluoromethanesulfonic (triflic) acid compared with aprotic methylene chloride and sulfolane solutions. The enhanced reactivity is discussed in terms of better solubility and higher dissociation of the nitronium salts, as
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4. Attempted hydrogen–deuterium exchange of the protio-trimethyloxonium dication (CH3)3OH2+, study of methylating ability of (CH3)3O+ in superacids and theoretical investigations
Attempted hydrogen–deuterium exchange of trimethyloxonium ion, (CH3)3O+ with excess of 1:1 2HF/SbF5 superacid at −30°C over a period of 30 days showed no exchange. Theoretical calculations at the MP2/6–31G** level are in accord with the lack of hydrogen–deuterium exchange in the methyl group of the (CH3)3O+ cation as protonation (protosolvation) pre
The National Academy of Sciences.