Abstract:In the present study, perlite was thermally activated and then modified desirably to generate super acidity by loading different weight percentages of sulfated zirconia (SZ) via the two-step sol-gel method. As-prepared sulfated zirconia perlite (SZP) catalysts showed suitable catalytic potential in the vapor phase alkylation of o, m, and p-cresols with tert-butyl alcohol. The presence of crystalline phases in SZP catalysts was confirmed by XRD and FT-IR studies. TEM images revealed the nano size of the catalys… Show more
“…Figure 7 shows the UV-Vis spectra of EP and PhEP (a), EP/PhBR and PhEP/PhBR composites (b), and PhBR (c). In the UV-Vis spectra of both EP and PhEP samples, peaks characteristic of aluminosilicates and explaining the presence of silica were observed at wavelengths of 254 nm and 243 nm, respectively [25]. As can be seen from Figure 7a, after the OxCh reaction of EP, the observed peak at 254 nm shifted to lower wavelengths (243 nm), and visible-light absorption improved.…”
The article presents a method for obtaining new composites using the well-known mineral expanded perlite (EP), and the industrial polymer butadiene rubber (BR). For the design of composites, a joint oxidative chlorophosphorylation reaction of BR and EP (as well as BR and modified EP) was carried out, and the modifications resulting from these reactions were further hydrolyzed. The structure and morphology of the obtained samples were characterized in detail using Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, X-ray powder diffraction, as well as scanning electron microscopy, and energy-dispersive X-ray analysis. EP and BR were separately modified with a similar reaction and characterized for data interpretation.
“…Figure 7 shows the UV-Vis spectra of EP and PhEP (a), EP/PhBR and PhEP/PhBR composites (b), and PhBR (c). In the UV-Vis spectra of both EP and PhEP samples, peaks characteristic of aluminosilicates and explaining the presence of silica were observed at wavelengths of 254 nm and 243 nm, respectively [25]. As can be seen from Figure 7a, after the OxCh reaction of EP, the observed peak at 254 nm shifted to lower wavelengths (243 nm), and visible-light absorption improved.…”
The article presents a method for obtaining new composites using the well-known mineral expanded perlite (EP), and the industrial polymer butadiene rubber (BR). For the design of composites, a joint oxidative chlorophosphorylation reaction of BR and EP (as well as BR and modified EP) was carried out, and the modifications resulting from these reactions were further hydrolyzed. The structure and morphology of the obtained samples were characterized in detail using Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, X-ray powder diffraction, as well as scanning electron microscopy, and energy-dispersive X-ray analysis. EP and BR were separately modified with a similar reaction and characterized for data interpretation.
“…The % selectivity of 2-TBC increased when the molar ratio increased from 1 to 2, and this increase became negligible afterwards. The % selectivity of 2,6-DTBC increased when increasing the concentration of tert-butyl alcohol due to the greater resident time of the mono tert-butylated product on the catalyst surface [33]. As the conversion of p-cresol and the selectivity toward 2-TBC are higher at a molar ratio of p-cresol to tertiary butanol of 1:2, the optimum molar ratio was fixed at 1:2.…”
Section: Effect Of Molar Ratio Of Tert-butyl Alcohol To P-cresolsmentioning
confidence: 99%
“…Sarish et al studied the alkylation of p-cresol with tertbutanol over WOx/ZrO 2 catalysts and the corresponding catalytic activity, which was compared with sulfated zirconia and zeolites like USY, H, and montmorillonite K-10, under optimized reaction conditions and concluded that the activity of sulfated zirconia was lower than that of the WO 3 /ZrO 2 catalyst [32]. Malpani et al designed a perlite-supported sulfated zirconia catalyst for the alkylation of isomeric cresols with tert-butyl alcohol, and the study revealed better conversion with few limitations [33].…”
12-Tungstophosphoric acid supported on nanosilica (TPA/SiO2) was employed as a catalyst for the tertiary butylation of p-cresol using tertiary butanol as an alkylating agent. The TPA/SiO2 catalyst was synthesized using the wet impregnation method followed by steaming at 150 °C for 6 h. The catalysts were characterized by means of X-ray diffraction (XRD) and Transmission Electron Microscopy (TEM) analysis. The surface acidity of the untreated and steamed catalysts was characterized via FTIR and DSC thermal analysis using pyridine as a probe molecule. The fresh and spent catalysts were characterized via TGA analysis. The catalytic activity studies showed that the steamed catalyst displayed higher activity, with a higher desired yield of 2-tert-butyl cresol (2-TBC) compared to the untreated catalyst, and that this activity was related to the presence of stronger Brønsted acid sites in the steamed catalyst. A detailed analysis of the TPA/SiO2 steamed catalyst was performed to study the effects of reactant time-on-stream, reactant feed rate, reaction temperature, and the molar ratio of tert-butanol to p-cresol. The optimum reaction temperature, tert-butanol/p-cresol molar ratio, feed rate, and time-on-stream were 413 K, a molar ratio of 2:1, 6 mL/min, and 2 h, respectively. The present study demonstrates that the TPA/SiO2 catalyst exhibits high activity in terms of % conversion and high % selectivity of 2-TBC under the optimized conditions. The characterization of fresh and spent catalysts confirmed the occurrence of coke deposition after the catalytic reaction. The catalyst was regenerated via heat treatment at 400 °C for 5 h. The regenerated catalyst was reused for subsequent runs for three cycles without showing a loss in its activity.
“…[9][10][11][12][13][14][15] Heterogeneous solid acids comprising diverse materials have been reported in the recent past for the production of tert-butylate m-cresol. Materials based on sulphated zirconia, 16 Al-MCM-41 molecular sieves, 17 Supported 12-tungstophosphoricacid and 12-tungstosilicicacid, 18 Perlite Supported Sulfated Zirconia, 19 12-tungstophosphoricacid and 12-tungstosilicicacid supported onto neutral alumina 20 are reported in the literature.…”
The present study reports nanocrystalline hierarchical zeoite ZSM‐5 as a potential alternative to homogeneous catalysts for the liquid phase tert‐butylation of m‐cresol. Polydiallyldimethylammonium chloride macro‐template was used to develop vacuum‐concentration dual template nano‐precursors by hydrothermal process. The catalytic performance was analyzed for the given reaction and the high percent conversion of reactants with excellent selectivity towards the ortho isomer, 2‐tert‐butyl‐5‐methylphenol was recorded. In contrast, the low activity and selectivity towards the tert‐butylation of m‐cresol, and the selectivity towards the desired product are noticed with the nanocrystalline zeolite ZSM‐5 synthesized without macro‐template. In addition, the catalyst is recoverable due to its robust nature, which indirectly reduces industrial wastage. Various parameters that affect the rate of the reaction were optimized. Kinetic analysis studies showed that the reaction followed first‐order kinetics with respect to tert‐ and the reaction obeyed the Langmuir‐Hinselwood mechanism. The activation energy was determined as 43.0 ± 0.2 kJ/mole. The study reveals that nanocrystalline hierarchical zeolite ZSM‐5 is an efficient, selective, simple, economical and environment‐friendly catalyst for the tert‐butylation of m‐cresol.
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