• Nem Talált Eredményt

24th International Symposium on Analytical and Environmental Problems

N/A
N/A
Protected

Academic year: 2022

Ossza meg "24th International Symposium on Analytical and Environmental Problems"

Copied!
1
0
0

Teljes szövegt

(1)

24th International Symposium on Analytical and Environmental Problems

426

SYNTHESIS AND CHARACTERIZATION OF 3D MESOPOROUS TRANSIENT METAL OXIDE FOR HIGH-PERFORMANCE CATALYSTS

Anett Gyuris, András Sápi

Department of Applied and Environmental Chemistry, University of Szeged, 6723 Szeged Rerrich Béla tér 1., Hungary,

e-mail: sapia@chem.u-szeged.hu, anett1224@hotmail.com

Keywords: Catalysts supports, Transient metal oxides, Hard template – Replica Method, Heterogeneous Catalysis

Different 3D mesoporous oxide materials (SiO2 – KIT-6, MCF-17, SBA-15, Co3O4, MnO2, Fe2O3, NiO, CeO2) prepared by the soft and hard template (replica) method due to the fact that the usage of the 3D mesoporous oxide supports

with high specific surface area has great influence on the catalytic activity and selectivity (e.g. Co3O4 supported catalyst is 10 times more active compared to the SiO2

supported Pt.).

The synthesis of KIT-6 is as follows: P123 (Pluronic-123) was homogenized in deionized water and cc. HCl and then butyl alcohol was added. This mixture was stirred for 1 hour at 35 0C. After 1 hour we were poured 58g TEOS (Tetraethyl orthosilicate) and stirred for 24 hours. After the material was dried we were filtered. The next day was calcined at 550 0C for 6 hours.

Furthermore Co3O4, MnO2, Fe2O3, NiO, CeO2

mesoporous oxide carriers were prepared. For the synthesis metal-nitrate was dissolved in deionized water. The prepared mesoporous KIT-6 silica were dissolved in toluene and all of it was stirred at 65 0C. The material was dried at 60 °C overnight then it was calcined at 300 °C for 6 hours. After the silica template was removed with NaOH solution and we were washed several times with deionized water and dried.

The synthesis of these mesoporous oxide carriers were successful and had large surface area. This fact was supported by TEM, BET and XRD monitoring prove.

Fig. 1. TEM images of KIT-6

Fig. 2. TEM images of NiO (A), Co3O4

(B), CeO2 (C), MnO2 (D)

Hivatkozások

KAPCSOLÓDÓ DOKUMENTUMOK

It is shown, that by varying the treatment distance and the initial Ar/N 2 /O 2 mixture composition of the surface-wave microwave discharge the concentration ratio of NO 3 − and H 2 O

The thermal decomposition of ammonium hydroxodisulphitoferriate(III), (diammonium catena- {bis( 2 -sulfito-O,O)- 2 -hydroxo-}ferrate(III) monohydrate), (NH 4 ) 2 [Fe(SO 3 )

KOLUMBÁN VILMOS JÓZSEF: EPERJESI ZSIGMOND ÉS KERESZTES MÁTÉ LEVELE 197 átaljában meghatározta vala, hogy a lutheránusokot, kik az Augustana Confessio mellől

In 2002 a fractionation procedure based on the application of supercritical CO 2 , subcritical H 2 O and of a mixture of subcritical H 2 O/CO 2 was proposed, which allowed

Adsorption kinetics of isoproturon has been studied by commonly used kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model and the

[r]

Deczki Sarolta Görföl Balázs Imre Zoltán Karsai György Kiss Attila Atilla Kiss Gabriella Matuska Ágnes Mészáros Zsolt R Müller Péter Reuss Gabriella Tóth Orsolya

HOp)la,lbHblX парафllНОВ, с другой стороны, отсутствпе~! н-парафинов в ненор~шльноii фракции. Для подтверждения вышесказанного бы;ш использованы