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This paper introduces a new high-octane gasoline blending component made from low value mixed butenes using a new process.
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In the present paper we report on the mechanism of i-butane alkylation by butenes using three types of well defined catalysts.
The dimerisation of 1-butene using (cod Ni(hfacac) 1 as catalyst has been investigated in different chloroaluminate ionic liquids.
Plans for the first large-scale demonstration plant to produce isobutene from n-butenes using ferrierite as catalyst have already been announced in the United States.
For the kinetic trends of the selective hydrogenation of 3,4-epoxy-1-butene using dendrimer-derived PtX (X = Ru, Pd) bimetallic catalysts, this also showed an enhanced catalytic behavior (in some cases) compared with catalysts prepared from traditional wet impregnation of metal salts.
Our previous work has focused on developing a physiologically based toxicokinetic (PBTK) model for BD to estimate its metabolic rate to 1,2-epoxy-3-butene (EB), using exhaled breath BD concentrations in human volunteers exposed by inhalation.
Mixed methods were used.
A mixed design was used.
Concurrent mixed methods were used.
Linear mixed models were fitted using ASREML.
Acidic materials (zeolites, supported acids) were screened for the alkylation of 3-methylthiophene (3MT) with 2-methyl-2-butene (2M2B), used as model reaction.
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