Postdoctoral research carried out at
The Royal Institution of Great Britain
Davy-Faraday Research Laboratory
(1995-96)
1. Characterisation of silico-alumino-phosphate molecular sieves (SAPO). Use of forcefield simulations intended to understand the catalytic properties of these materials.

AlPO-5 structure
Initially, the structure of these (crystalline) materials can be considered
as an AlPO (alumino-phosphate) framework...
Some considerations about AlPOs...
AlPO frameworks contain tetrahedrically coordinated Al and P (TO4 units, where T=Al,P), edged linked forming -T1-O-T2- units in which there is a strict structural alternance between Al & P: that means if T1=Al, then T2=P; or to put it another way the first T environments of Al and P are: P(4Al), and Al(4P). This fact is frequently refered to as 'ordered material', because no Al-O-Al, or P-O-P ever appear, as it should happen in a 'random' distribution for Al & P in the network. This has important consequences in the configurational entropy of the material about which I can tell you privately because I don't want to bother you too much.Two more things about AlPOs: they don't have cations to compensate the structure (unlike zeolites) and therefore they don't have either Bronsted acid sites. Consequence of that: they are not very reactive in catalysis. Well, they can have Lewis acidity but you have much better materials in this regard. The second thing is: what about the structure of these materials?. Well, they also microporous like zeolites...
Structure of zeolites. Flexibility of TOT (T=Si,Al) angles allow formation
of different rings with 4, 5, 6, 8, 10, etc members which gives raise to a
virtually infinite different structures with micropores and cavities in the
range 4-20 Angstroms, making zeolites microporous materials.
Some AlPOs have the same structures than some
zeolites (vg. AlPO-5 & SSZ-24; or SAPO-37 & Y; or SAPO-34 & chabazite), but
normally they have unique structures, microporous structures like zeolites but
with different pore systems. Therefore they are potentially atractive as acid
catalysts if we manage to create Bronsted acidity in the structure...
...but how to do that? (That's one of the topics of my research!)
...end of considerations about AlPOs
P-->Si,H and Al,P-->Si,Si substitutions in the framework. Let's see a scheme ...
Mechanisms 2 and 3 have been investigated with
computational techniques (Mechanism 1 is not experimentally observed).
The extent of both substitution mechanisms has a relation with the number and
location of the Bronsted acid centers in the material, which are responsible of
the use of the SAPO in acid catalysis.
A better understanding of these mechanisms can provide a good insight in the
selection of appropiate catalysts for industrial processes, according to their
structural and chemical properties.
2. Diffusion of C8 aromatics in a 10 and 12 Membered Rings Zeolite (CIT-1).
Use of forcefield Molecular Dynamics aimed to calculate self-diffusivities,
activation energies, and diffusion features: shape selectivity effects caused
by the two-channel microporous structure
and the different size of the guest molecules.
It is well known that two of the most iportant properties of zeolites are
their microporosity and acidity. The microporososity of these crystalline
materials is controlled in the synthesis process according to the pore
and channel size distribution of the structure. Channels are window openings
formed by 4,6,8,10,12, etc T(Si,Al) atoms. The more T atoms are forming the
channel the bigger it is. Channels of a given number of T atoms are slightly
different in size according to the structure in which they occur:
this is due to the different flexibility of the framework in the different
cases. In the figure above (AlPO-5 structure) you can see a view across a
12 MR channel.
CIT-1 structure.
The MD simulations have carried out with the general purpose DL_POLY code
in its paralell version implemented in a 512 PE CRAY-T3D. The results show
how para-xylene and ortho-xylene diffuse through the 12MR and 10MR channels
systems in [001] and [110] in CIT-1. It is seen how the slightly bigger ortho
isomer can not diffuse through the smaller 10MR channels although some
penetration into the channels is appreciated. The penetration into the 10MR
channels produces a decrease in the diffusivity of ortho-xylene which blocks
itself in these incursions. On the other hand the para isomer diffuses through
both 12MR and 10MR channels in CIT-1. In particular, diffusion through the
10MR channel proceeds quicker due to the impossibility to rotate in these
narrower 'corridors'. Curiously, the 10MR channels are slowing down
the diffusion of ortho-xylene and -at the same time- they are fastening
the diffusion of para-xylene.
CIT-1 presents new and interesting features for the diffusion processes of
C8 aromatics and provides a possible scenario for industrial applications.
Xylene (centre of mass trajectories) diffusing mainly through the 12MR
channels of the CIT-1 structure.
Activation energies have also been calculated, the results showing that the
para isomer diffuses with very similar activation energies through both
channels, and in the case of the ortho-xylene the activation energy
for the diffusion through 12MR is a bit higher than in the case of 'para'
but still allowing diffusion. In the case of ortho-xylene diffusing
through 10MR channels a very high activation energy, more than 100kcal/mol,
was obtained showing that no diffusion through these channels is possible.
Para-xylene trajectories in a 2-D projection through the CIT-1 structure.
It can be observed in both graphs how there are preferential diffusion in the
bigger 12MR channel but there is also some diffusion in the narrower 10MR
channel. Similar trajectories obtained for the bigger ortho-xylene isomer
show selective diffusion in the 12MR channel only.
This Project was funded by Ministerio de Educacion y Ciencia (Spain)
This postdoctoral project was conducted under Professor
C. R. A. Catlow