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Journal ArticleDOI

Partial oxidation of toluene by O2 over mesoporous Cr/AlPO

TL;DR: In this article, the prepn. of mesoporous Cr/AlPO was carried out under hydrothermal conditions and the catalyst was characterized by low angle XRD, N-adsorption, diffuse reflectance UV-visible spectroscopy, ESR and thermal anal.
About: This article is published in Catalysis Communications.The article was published on 2002-02-01 and is currently open access. It has received 34 citations till now. The article focuses on the topics: Partial oxidation & Catalysis.

Summary (2 min read)

1. Introduction

  • The incorporation of transition metal ions into the framework sites of microporous aluminosilicates and aluminophosphates has been reported in the literature and resulting systems are potential catalysts for various selective redox reactions [1– 3].
  • Cr– AlPO-5 was shown to be an active and recyclable catalyst for the oxidation of alkylbenzenes with either TBHP or O2 [7].
  • The potential of chromium containing *Corresponding author.
  • S1566-7367 (01 )00070-X catalysts can be increased by using molecular oxygen as oxidant and thereby carrying the reaction in vapour phase it is possible to control the leaching of chromium from the framework, also known as PII.

2.1. Synthesis

  • Mesoporous chromiumaluminophosphateswere prepared using cetyltrimethylammoniumbromide (CTAB) as surfactant and with the following gel composition.
  • Various sources of aluminium have been tried and aluminium hydroxide has been chosen as the source.
  • Chromium nitrate was used as transition metal precursor.
  • The pH of the gel was maintained at 9.5 with tetra methyl ammonium hydroxide, as the use of other sources like NaOH and NH4OH resulted only in the amorphous materials.
  • The solidwas filtered,washed several times with deionisedwater and calcined at 773K for 6 h to remove the organic template.

2.2. Experimental setup and procedure

  • The experimental setup consisted of three parts: the gas supply system, the reactor and the analysis system.
  • The feed was regulated through mass flow controllers.
  • The temperature was decreased and the flow was switched to the mixture of 2 vol% toluene plus 40-vol% O2 in Ar.

2.3. Characterisation of the catalyst and reaction products

  • Various techniques have been used for the characterisation of the materials synthesised.
  • Diffuse reflectance UV–VIS spectroscopy was carried out on a Cary 5E UV–VIS–NIR spectrophotometer.
  • X-ray photoelectron spectroscopic measurements (XPS) for Cr2p were performed on a PHI-550 ESCA-System (Perkin–Elmer GmbH).
  • A Blazers QMG-421 mass-spectrometer and a Perkin–Elmer Autosystem XL gas chromatograph were used for the gas phase analysis.
  • Ar=O2, CO, CO2 and H2O were analysed in a Carboxen-1010 capillary column and analysed by a TCD.

3.1. XRD

  • XRD patterns of as-synthesised and calcined AlPO, Cr–AlPO are shown in Fig. 1. XRD patterns of AlPO show low angle peaks typical for hexagonal phase.
  • The as-synthesised Cr–AlPO material shows a maximum intense peak corre- sponding to ð100Þ reflection followed by weaker but clear peaks corresponding to ð110Þ and ð200Þ reflections that can be indexed on the basis of a hexagonal lattice.
  • The sample retained its hexagonal structure after calcination.
  • With NaOH and NH4OH only amorphous materials were formed.
  • The function of organic ammonium cation from TMAOH is probably to modify the strength of the electrostatic interactions between the aluminophosphate species and the cationic surfactant micelle assembly to form the SþI =TMAþ ion pair.

3.2. Thermal analysis

  • Thermogram of as-synthesised ALPO shows mainly two weight loss regions one corresponding to loss of physi-sorbed water below 373 K.
  • The second and the main weight loss was observed in the temperature range 450–550 K corresponding to loss of organic template.

3.3. N2 adsorption

  • Nitrogen adsorption–desorption isotherms of the Cr–AlPO are shown in Fig. 2.
  • For all samples, the isotherms are similar having inflection around p=p0 ¼ 0:2–0.3 characteristic of mesoporous materials.
  • BET surface area and BJH pore size distribution for various catalysts are given in Table 1.
  • It was observed that Cr–ALPO exhibit type IV isotherm with a hysteresis characteristic of mesoporous material.

3.4. UV–VIS DRS

  • UV–VIS spectroscopy is a technique for the characterisation of transition–metal-incorporated zeolites [13–15].
  • Fig. 3 shows UV–VISDRS spectra of as-synthesised and calcined Cr–AlPO samples.
  • These bands are characteristic of trivalent chromium in octahedral co-ordination.
  • Due to the large difference in LFSE values of Cr(III) for tetrahedral (66.9 KJ/mol) and octahedral (224.5 KJ/mol) geometries, chromium atoms in as-synthesised material mainly occupy extra framework sites [16–18].

3.6. Catalytic activity

  • Table 2 gives typical results for the oxidation of toluene in the temperature range 523–648 K over Cr–AlPO catalyst.
  • Benzaldehyde, benzene, CO2 and CO are the reaction products.
  • It was observed that with the increase of the temperature, the conversion of the toluene and selectivity of benzene increased.
  • Coke formation was not detected to any significant extent.

4. Conclusions

  • Cr–AlPO materials have been prepared by hydrothermal synthesis and found to have hexagonal MCM-41 like morphology.
  • These materials have high surface area 500 m2=g and pores are in mesoporous range 29 A. UV–VIS and ESR techniques have confirmed the presence of Cr5þ=6þ in the framework.
  • Cr–AlPO catalysts have been shown to be active for the vapour phase oxidation of toluene with molecular oxygen.
  • It has been observed that in Cr–AlPO both acidity (due to Al3þ) and redox properties (due to Cr5þ=6þ) are competing leading to benzene and benzaldehyde, respectively.

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Citations
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Journal ArticleDOI
TL;DR: In this article, pure ZnO and g-C3N4 were synthesized using coprecipitation and simple calcination methods, respectively, and impregnated on a g-c3n4 surface with 10, 20 and 30 weight percentages, respectively.
Abstract: In this study, pure ZnO and g-C3N4 were synthesized using coprecipitation and simple calcination methods, respectively. Further, ZnO is impregnated on a g-C3N4 surface with 10, 20 & 30 weight percentages, respectively. Besides, these materials are characterized by various physicochemical techniques such as PXRD, UV-Vis-DRS, TEM, PL, and FT-IR, etc. Vitally, as-prepared materials, catalytic activity was tested for removal of Rhodamine B and 4-nitrophenol from the wastewater under visible light irradiation. Among all these catalysts, 20 wt% ZnO/g-C3N4 showed better activity and showed 67% and 75% mineralization. The graphical abstract simply represents the proposed mechanism for photocatalytic removal of 4-nitrophenol and Rhodamine B with ZnO/g-C3N4 composite. ZnO was a hexagonal plate type structure and g-C3N4 shows a sheet-type structure.

7 citations

Journal ArticleDOI
TL;DR: An NTP hybrid system was designed in combination with metal oxide (MOX)-coated glass beads (GB) to synthesize value-added fuels and chemicals directly from methane.
Abstract: An NTP hybrid system was designed in combination with metal oxide (MOX)-coated glass beads (GB) to synthesize value-added fuels and chemicals directly from methane. The combined plasma-packed mode was found to be a promising alternative to thermal catalysis, as it successfully enabled the single-step partial oxidation of methane to produce liquid oxygenates at atmospheric pressure and room temperature. When comparing plasma without packing (58%) and MOX/GB coupled plasma mode, the later method enhances the liquid selectivity to 74% with the introduction of C2 oxygenates in addition to C1 chemicals. Among the coated materials applied, NiO-coated GBs showed the highest liquid yield of ∼10%, including the maximum methanol yield of ∼5%, while coupled with NTP-DBD mode. Gas discharge-promoted methane conversion was observed in the presence of GB and MOX/GB, which can be attributed to the enhanced electric field generated as a result of the improved plasma strength created by the beads. Also, the oxide layer of metal oxide nanoparticles provides a catalytic base for adsorption/desorption of methane and other gas phase active species, which can facilitate the partial oxidation process of methane either by the gas-phase active oxygen species or through the interaction of surface hydroxyl groups.

7 citations

Journal ArticleDOI
Gao Biao1, Luo Yajun1, Miao Changxi2, Yue Yinghong1, Yang Weimin2, Hua Wei-Ming1, Gao Zi1 
TL;DR: In this article, a series of Cr-SiO2 catalysts with a mass fraction ranging from 0.5% to 9% were prepared by a solgel method, and their catalytic behavior in the dehydrogenation of 1-butene to 1,3-butadiene (BD) using CO2 as a soft oxidant was studied.

7 citations

Reference EntryDOI
13 May 2011
TL;DR: Aluminophosphate molecular sieves exhibit structural and compositional diversity and can be modified by other elements, thus providing novel SAPO, MAPO, and MAPSO materials as mentioned in this paper.
Abstract: Aluminophosphate molecular sieves exhibit structural and compositional diversity. Their frameworks can be modified by other elements, thus providing novel SAPO, MAPO, and MAPSO materials. They possess the characteristics of both zeolites and aluminophosphates all of which result in unique catalytic, ion-exchange, and adsorbent properties. Aluminophosphate molecular sieves have been prepared hydrothermally in nonaqueous reaction media. The crystallization process depends on a number of variables including temperature, time, molar ratio of the reactants, and pH. The most commonly investigated metal ions incorporated into aluminophosphate frameworks are transition metal ions of first transition series. Different characterization techniques are used for studying their oxidation number, location, and coordination environment within aluminophosphate frameworks. These parameters, together with structural characteristics of the framework such as pore size, pore shape, and geometry, significantly affect the catalytic performance of aluminophosphate materials. Methanol to olefin conversion and oxidation reactions are instances of industrially important reaction systems where aluminophosphate molecular sieves demonstrate an important catalytic performance. Keywords: aluminophosphates; molecular sieves; open-framework structures; templating role; organic templates; hydrothermal synthesis; isomorphous substitution; transition metal ions; catalysis; methanol to olefin conversion; oxidation reactions; SAPO; MAPO; MAPSO

6 citations

Journal ArticleDOI
TL;DR: In this paper, the gas phase cyclohexanol and air reaction over Mn-MCM-41 molecular sieve was studied for the first time, and the conversion is almost constant even up to 5 h, and follows a parabolic behavior with respect to temperature.
Abstract: Mn–MCM-41 was synthesized by the hydrothermal method. The synthesized material was characterized by various physicochemical techniques such as small angle X-ray diffraction, elemental analysis, Fourier transform infrared spectroscopy and diffuse reflectance ultraviolet–visible spectroscopy. The gas-phase cyclohexanol and air reaction over Mn–MCM-41 molecular sieve was studied for the first time. The conversion is almost constant even up to 5 h, and follows a parabolic behavior with respect to temperature. The conversion reaches a maximum at 350 °C and selectivity towards cyclohexene is increased with temperature. The conversion and cyclohexene selectivity were increased with flow rate.

6 citations

References
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Journal ArticleDOI
TL;DR: This work focuses on the surface chemistry and spectroscopy of chromium in inorganic oxides and the mechanics of hydrogenation-dehydrogenation reactions.
Abstract: Focuses on the surface chemistry and spectroscopy of chromium in inorganic oxides. Characterization of the molecular structures of chromium; Mechanics of hydrogenation-dehydrogenation reactions; Mobility and reactivity on oxidic surfaces.

728 citations

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01 Oct 1988
TL;DR: In this article, the authors present an interpretation of phase diagram for phase diagrams and demonstrate the properties of the phase diagram in terms of magnetic and optical properties, as well as non-stoichiometry.
Abstract: Crystal Structures. Bonding in Solids. Crystallography and Diffraction Techniques. Other Techniques: Microscopy, Spectroscopy, Thermal Analysis. Crystal Defects, Non--Stoichiometry and Solid Solutions. Interpretation of Phase Diagrams. Electrical Properties. Magnetic and Optical Properties. Synthesis Methods. Further Reading. Appendices. Questions. Index.

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Book ChapterDOI
TL;DR: In this article, the surface characterization of silicalite and titanium-silicalite is made by combined use of IR and UV-Vis reflectance spectroscopy, and the nature of the IR modes and of the electronic transitions associated with framework titanium is discussed in detail.
Abstract: Surface characterization of silicalite and titanium-silicalite is made by combined use of IR and UV-Vis reflectance spectroscopy. The nature of the IR modes and of the electronic transitions associated with framework titanium is discussed in detail. The perturbation caused by the adsorption of small polar molecules (H 2 O, NH 3 , CH 3 OH) on both the IR and UV-Vis spectra is discussed in terms of the formation of six-coordinated complexes by ligand insertion in the Ti(IV) coordination sphere. All the Ti(IV) is accessible to the interaction with the molecules.

392 citations

Journal ArticleDOI
TL;DR: In this article, the mesoporous Ti-, Cr- and V-substituted derivatives of the cubic silica molecular sieve MCM-48 have been synthesized at 373 K by an electrostatic assembly pathway using cetyltrimethylammonium cation as the templating agent.
Abstract: Mesoporous Ti-, Cr- and V-substituted derivatives of the cubic silica molecular sieve MCM-48 have been hydrothermally synthesized at 373 K by an electrostatic assembly pathway using cetyltrimethylammonium cation as the templating agent. The transition metal substituted products all exhibit improved crystallinity and a narrower pore size distribution relative to the pristine molecular sieve. Transition metal substitution caused an enlargement of the cubic unit cell as well as an increase in the degree of crosslinking in the mesopore walls. The coordination of V-sites in the meso-structure is exclusively tetrahedral, as judged by NMR spectroscopy. These sites as well as those of Ti and Cr sites are active and selective for the peroxide oxidation of styrene and methyl methacrylate to benzaldehyde and methyl pyruvate, respectively.

141 citations

Journal ArticleDOI
TL;DR: In this paper, a mechanism involving initial free radical autoxidation of the hydrocarbons followed by selective CrAPO-5-catalyzed intramolecular, heterolytic decomposition of the secondary alkyl hydroperoxide intermediate to the corresponding ketone and water is presented.

123 citations

Frequently Asked Questions (20)
Q1. What contributions have the authors mentioned in the paper "Partial oxidation of toluene by o2 over mesoporous cr–alpo" ?

Viswana et al. this paper used mesoporous Cr-AlPO for partial oxidation of toluene with molecular oxygen in vapour phase. 

The formation of benzene, as a result of dealkylation reaction predominates on acid ðAl3þÞ sites, whereas on redox sites ðCr5þ=6þÞ oxidation of toluene is taking place leading to benzaldehyde. 

The incorporation of transition metal ions into the framework sites of microporous aluminosilicates and aluminophosphates has been reported in the literature and resulting systems are potential catalysts for various selective redox reactions [1– 3]. 

The function of organic ammonium cation from TMAOH is probably to modify the strength of the electrostatic interactions between the aluminophosphate species and the cationic surfactant micelle assembly to form the SþI =TMAþ ion pair. 

But for the large-scale production of fine chemicals, replacement of conventional homogeneous systems by heterogeneous catalysts will be advantageous inthe sense of catalyst recovery and reduction of undesirable side reactions. 

With the recent discovery of mesoporous materials, the activities of chromium containing MCM-41, MCM-48, HMS have been tested for the oxidation of alkylbenzenes with peroxides as oxidants [8–10]. 

If either NaOH or NH4OH is used, the smaller cations Naþ, NHþ4 compete with the aluminophosphate species and thus restrict the interaction with the positively charged cationic surfactant. 

The decrease in the surface area of the Cr– AlPO compared to AlPO could be due to partial loss of crystallinity, which is in agreement with the observation from XRD. 

PII: S1566-7367 (01 )00070-Xcatalysts can be increased by using molecular oxygen as oxidant and thereby carrying the reaction in vapour phase it is possible to control the leaching of chromium from the framework. 

ESR spectra of calcined Cr–AlPO shows g value at 1.95 characteristic of pentavalent chromium in tetrahedral or distorted tetrahedral co-ordination. 

The pH of the gel was maintained at 9.5 with tetra methyl ammonium hydroxide, as the use of other sources like NaOH and NH4OH resulted only in the amorphous materials. 

As stated earlier, aluminium hydroxide may form a less polymerised aluminophosphate with many hydroxyl groups and favour the assembly of the mesostructure compared to other aluminium sources [11,12]. 

the potential of chromium containing porous solid catalysts in liquid phase is limited because of the leaching of the active metal from framework. 

Pore size ( A) Pore volume (cc/g)AlPO 34.5 33.0 38.10 685 28 0.65 Cr–AlPO 35.0 33.4 38.56 490 29 0.51Cr–AlPO materials have been prepared by hydrothermal synthesis and found to have hexagonal MCM-41 like morphology. 

Mesoporous chromiumaluminophosphateswere prepared using cetyltrimethylammoniumbromide (CTAB) as surfactant and with the following gel composition. 

The low angle X-ray diffraction pattern of the sample was recorded on a Siemens D 500 ðh=2hÞ using monochoromatised Cu-Ka radiation ðk ¼ 1:5406 AÞ with a scan speed of 1 /min over the range 2 < 2h < 10 . 

In both the cases the pore size is around 29 A.UV–VIS spectroscopy is a technique for the characterisation of transition–metal-incorporated zeolites [13–15]. 

4. As-synthesised material shows a broad singlet with a g value of 1.98 indicating Cr3þ ions in octahedral co-ordination [20,21]. 

In this communication, the synthesis, characterisation and catalytic activity of mesoporous Cr–AlPO for toluene oxidation with molecular oxygen are reported. 

CO, CO2 and H2O were analysed in a Carboxen-1010 capillary column and analysed by a TCD.XRD patterns of as-synthesised and calcined AlPO, Cr–AlPO are shown in Fig. 1. XRD patterns of AlPO show low angle peaks typical for hexagonal phase.