Thornton et al., 1974 - Google Patents
Catalysis by matrix-bound sulfonic acid groups: olefin and paraffin formation from butyl alcoholsThornton et al., 1974
- Document ID
- 1402918575774160211
- Author
- Thornton R
- Gates B
- Publication year
- Publication venue
- Journal of Catalysis
External Links
Snippet
Catalysis by a poly (styrene-divinylbenzene) matrix containing-SO 3 H groups was characterized by reaction rates and product distributions for reactions of isopropyl, isobutyl, and s-butyl alcohols at about 100° C. Infrared spectra of functioning catalyst membranes …
- -1 butyl alcohols 0 title abstract description 24
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/03—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
- C07C29/04—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Thornton et al. | Catalysis by matrix-bound sulfonic acid groups: olefin and paraffin formation from butyl alcohols | |
Kunin et al. | Macroreticular ion exchange resins | |
Ancillotti et al. | Ion exchange resin catalyzed addition of alcohols to olefins | |
Oost et al. | The synthesis of tertiary amyl methyl ether (TAME): microkinetics of the reactions | |
US1999620A (en) | Process for the manufacture of alcohols | |
Ono et al. | Mechanism of methanol conversion into hydrocarbons over ZSM-5 zeolite | |
US4340769A (en) | Process for the continuous production of lower aliphatic alcohols | |
Velo et al. | Inhibition by product in the liquid-phase hydration of isobutene to tert-butyl alcohol: kinetics and equilibrium studies | |
Fǎrcaşiu et al. | Strength of solid acids and acids in solution. Enhancement of acidity of centers on solid surfaces by anion stabilizing solvents and its consequence for catalysis | |
KR100266914B1 (en) | Olefin hydration process | |
Tejero et al. | Scope and limitations of mechanistic inferences from kinetic studies on acidic macroporous resins The MTBE liquid-phase synthesis case | |
CA1185273A (en) | Process for the preparation of pure tert.-olefins | |
US3920582A (en) | Solid catalyst for heterogeneous reactions | |
Izquierdo et al. | Kinetic study of isobutene dimerization catalyzed by a macroporous sulphonic acid resin | |
Gates et al. | The dehydration of formic acid catalyzed by polystyrene sulfonic acid | |
Uematsu | The Isomerization of n-Butenes over Acidic Ion-exchange Resin | |
Pääkkönen et al. | Comparative study of TAME synthesis on ion-exchange resin beads and a fibrous ion-exchange catalyst | |
Weller et al. | The Effect of Pretreatment on the Activity of Gamma-Alumina. II. Hydrogen–Deuterium Exchange | |
Oktar et al. | Etherification rates of 2‐methyl‐2‐butene and 2‐methyl‐1‐butene with ethanol for environmentally clean gasoline production | |
Buttersack et al. | Sulfonic acid ion-exchange resins as catalysts in nonpolar media: II. Influence of conditioning methods on the acidity and catalytic activity | |
US5220087A (en) | Preparation of strong and super acid catalysts using elemental fluorine | |
US4123379A (en) | Production of very strongly acidic solids for hydrocarbon conversions | |
US6211408B1 (en) | Method of removing iodides from non-aqueous organic media utilizing silver or mercury exchanged macroporous organofunctional polysiloxane resins | |
Matsuda et al. | Selectivity in ethylene dimerization over supported nickel oxide catalysts | |
Kramer | Hydride transfer reactions in concentrated sulfuric acid |