2004
DOI: 10.1016/j.catcom.2004.03.005
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A “one-pot” synthesis of adipic acid from cyclohexene under mild conditions with new bifunctional Ti-AlSBA mesostructured catalysts

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Cited by 49 publications
(25 citation statements)
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“…(A). The pure SBA‐15 sample exhibits a type IV isotherm with sharp uptake of nitrogen in the p/p 0 range 0.6–0.8 indicating the presence of mesoporous hexagonal structure with ordered porosity . Interestingly, the SBA‐15 supported copper catalysts show similar isotherms to that of SBA‐15.…”
Section: Resultsmentioning
confidence: 92%
“…(A). The pure SBA‐15 sample exhibits a type IV isotherm with sharp uptake of nitrogen in the p/p 0 range 0.6–0.8 indicating the presence of mesoporous hexagonal structure with ordered porosity . Interestingly, the SBA‐15 supported copper catalysts show similar isotherms to that of SBA‐15.…”
Section: Resultsmentioning
confidence: 92%
“…In the reported batch procedures, the direct oxidation of cyclohexene to adipic acid requires several hours to obtain full conversion [9][10][11][12][13][14]. In flow, the reaction could be accelerated significantly by utilizing harsh reaction conditions, i.e., a reaction temperature of 100°C and the use of a highly concentrated hydrogen peroxide solution (50 %) resulted in the formation of adipic acid (50 wt % isolated yield) within 20 min.…”
Section: Residence Timementioning
confidence: 99%
“…Hydrogen peroxide has a high active oxygen content (47 % active oxygen) and produces water as the sole byproduct [7]. Inspired by this landmark paper, several other catalysts have been developed with varying success to enable efficient adipic acid synthesis starting from cyclohexene [9][10][11][12][13][14]. One of the first reports was provided by Noyori and co-workers [8].…”
Section: Introductionmentioning
confidence: 99%
“…For example, Cr-MCM-41, Cr-MCM-48 [15], W-SBA-15 [16], Ti-AlSBA [17], TiO 2 -SiO 2 [18] and RuO 2 /TiO 2 [19] have been employed as catalysts for the allylic oxidation or epoxidation of CHE with tert-butylhydroperoxide or H 2 O 2 . The major products of the epoxidation of CHE are cyclohexene oxide (epoxide) and 1,2-cyclohexanediol (CHDL) [18][19][20].…”
Section: Introductionmentioning
confidence: 99%