Title of Invention

A PROCEES FOR THE PREPARATION OF PYROGENIC SILICON-TITANIUM MIXED OXIDE POWDER

Abstract Process for the preparation of a pyrogenic silicon-titanium mixed oxide powder having a BET surface area is 200 to 400 m2 /g, silicon dioxide content of 97.0 ± 1.5% by weight, titanium dioxide content of 3.5 ± 1.0% by weight and the sum of silicon dioxide content and titanium dioxide content being greater than 99.7% by weight, all percentages by weight relating to the total amount of the powder, said process is characterized in that 97.0 ±1.5 parts by weight calculated as SiO2 of silicon halide and 3.5 ±1.5 parts by weight calculated as TiO2 of titanium halide are evaporated, the vapours are taken to a mixing chamber, hydrogen and primary air are taken to the mixing chamber separately therefrom, the mixture of the vapours of silicon halide and titanium halide, hydrogen- containing combustible gas and primary air is subsequently ignited in a burner and the flame is burned into a reaction chamber, secondary air is additionally introduced into the reaction chamber, the solid is subsequently separated from gaseous substances, and the solid is subsequently freed as far as possible from halide-containing substances by treatment with steam at temperatures of 250 to 700°C the amount of the required substances consisting of silicon chloride, titanium chloride, combustible gas, primary air and secondary air being chosen such that an adiabatic flame temperature Tad results, for which the following is true: 900°C < Tad < 1200°C, with Tad = temperature of required substances + sum of the reaction enthalpies of the partial reactionslhead capacity of the substances which leave the reaction chamber, comprising silicon dioxide, water, hydrogen chloride, if appropriate carbon dioxide, oxygen, nitrogen, and if appropriate of the carrier gas if this is not air or nitrogen, the specific heat capacity of these substances at 1000°C being used as a basis.
Full Text Silicon-titanium mixed oxide powder, dispersion thereof and
titanium-containing zeolite prepared therefrom
The invention relates to a pyrogenic silicon-titanium mixed
oxide powder and its preparation.
The invention furthermore relates to a dispersion
comprising the pyrogenic silicon-titanium mixed oxide
powder.
The invention furthermore relates to processes for the
preparation of a titanium-containing zeolite by means of
the pyrogenic silicon-titanium mixed oxide powder or of a
dispersion comprising this powder. The invention
furthermore relates to the titanium-containing zeolites
obtainable by these processes and to their use as a
catalyst.
The use of silicon-titanium mixed oxide powders for the
preparation of titanium-containing zeolites is known from
EP-A-814058. Titanium-containing zeolites are efficient
catalysts for the oxidation of olefins using hydrogen
peroxide. They are obtained by hydrothermal synthesis
starting from silicon-titanium mixed oxide powders in the
presence of a template. In EP-A-814058, it is disclosed
that pyrogenic silicon-titanium mixed oxides having a
silicon dioxide content of 75 to 99.9% by weight and a
titanium dioxide content of 0.1 to 25% by weight can be
employed for this. A composition which contains from 90 to
99.5% by weight of silicon dioxide and 0.5 to 5% by weight
of titanium dioxide is particularly advantageous. As
templates, amines, ammonium compounds or alkali/alkaline
earth metal hydroxides can be employed.
A disadvantage of the process disclosed in EP-A-814058 is
the long reaction time which is necessary for the reaction

of the silicon-titanium mixed oxide in the presence of the
template. Furthermore, not all titanium-containing zeolites
obtained according to EP-A-814058 show adequate catalytic
activity.
An object of the invention was therefore to make available
a silicon-titanium mixed oxide, with which the reaction
times in the preparation of the titanium-containing zeolite
can be reduced. A further object of the invention was to
make available a titanium-containing zeolite having a high
catalytic activity.
The invention relates to a pyrogenic silicon-titanium mixed
oxide powder, which has
- a BET surface area of 200 to 400 m2/g,
- a silicon dioxide content of 97.0 ± 1.5% by weight,
- a titanium dioxide content of 3.5 ± 1.0% by weight and
- in which the sum of silicon dioxide content and titanium
dioxide content is greater than 99.7% by weight,
all percentages by weight relating to the total amount of
the powder.
Pyrogenic is to be understood as meaning metal mixed oxide
particles obtained by flame oxidation and/or flame
hydrolysis. In this process, oxidizable and/or hydrolysable
starting, substances are as a rule oxidized or hydrolysed in
a hydrogen-oxygen flame. The metal mixed oxide particles
according to the invention are as far as possible pore-free
and have free hydroxyl groups on the surface. They are
present in the form of aggregated primary particles.
It has been shown that a high BET surface area markedly
reduces the period of time for the preparation of a
titanium-containing zeolite from the silicon-titanium mixed
oxide powder according to the invention.

A silicon-titanium mixed oxide powder according to the
invention having a BET surface area of 250 to 350 m2/g is
preferred and particularly preferably one of 300 ± 30 m2/g.
Furthermore, a silicon-titanium mixed oxide powder having a
silicon dioxide content of 97.0 ± 1.0% by weight and a
titanium dioxide content of 3.5 ± 0.75% by weight is
preferred where the sum of silicon dioxide content and
titanium dioxide content is greater than 99.9% by weight. A
silicon-titanium mixed oxide powder having a silicon
dioxide content of 97.0 ± 0.5% by weight and a titanium
dioxide content of 3.5 ± 0.5% by weight is particularly
preferred where the sum of silicon dioxide content and
titanium dioxide content is greater than 99.9% by weight.
The sum of silicon dioxide content and titanium dioxide
content in the powder according to the invention is greater
than 99.7% by weight and preferably greater than 99.9% by
weight. The content of the metals Al, Ca, Co, Fe, K, Na, Ni
and Zn is preferably less than 50 ppm each and particularly
preferably less than 25 ppm each. The content of chloride
is preferably less than 7 00 ppm. It has proved advantageous
for the preparation of titanium-containing zeolites if the
contents of these metals and chloride do not exceed these
values. These impurities can originate from the required
substances and/or can be caused due to the process.
A further subject of the invention is a process for the
preparation of the silicon-titanium mixed oxide powder
according to the invention in which
- 97.0 ± 1.5 parts by weight calculated as SiO2 of a
silicon chloride and 3.5 ± 1.0 parts by weight calculated
as TiO2 of a titanium chloride are evaporated, the
vapours are taken to a mixing chamber, hydrogen and
primary air are taken to the mixing chamber separately
therefrom,

- the mixture of the vapours of silicon chloride and
titanium chloride, hydrogen-containing combustible gas
and primary air is subsequently ignited in a burner and
the flame is burned into a reaction chamber,
- secondary air is additionally introduced into the
reaction chamber, the solid is subsequently separated
from gaseous substances, and
- the solid is subsequently freed as far as possible from
halide-containing substances by treatment with steam at
temperatures of 250 to 700°C
- the amount of the required substances consisting of
silicon chloride, titanium chloride, combustible gas,
primary air and secondary air being chosen such that an
adiabatic flame temperature Tad results, for which the
following is true:
900°C with
Tad = temperature of required substances + sum of the
reaction enthalpies of the partial reactions/heat
capacity of the substances which leave the reaction
chamber, comprising silicon-titanium mixed oxide, water,
hydrogen chloride, if appropriate carbon dioxide, oxygen,
nitrogen, and if appropriate of the carrier gas if this
is not air or nitrogen, the specific heat capacity of
these substances at 1000°C being used as a basis.
The specific heat capacities can be determined, for
example, with the aid of the VDI Warmeatlas [VDI heat
atlas] (Chapter 7.1 to 7.3 and 3.7, 8th Edition).
The reaction of the silicon chlorides and titanium
chlorides in the presence of oxygen and of a combustible
gas yields silicon-titanium mixed oxide, water,
hydrochloric acid and, in the case of carbon-containing
silicon and/or titanium compounds and/or carbon-containing

combustible gases, carbon dioxide. The reaction enthalpies
of these reactions can be calculated by means of standard
works known to the person skilled in the art.
In Table 1, some selected values of reaction enthalpies of
the reaction of silicon halides and titanium tetrachloride
in the presence of hydrogen and oxygen are given.
Methyltrichlorosilane (MTCS, CH3SiCl3) , trichlorosilane
(TCS, SiHCl3) and/or dichlorosilane (DCS, SiH2Cl2) and
titanium tetrachloride can particularly preferably be
employed.

Suitable combustible gases are hydrogen, methane, ethane,
propane and/or natural gas, hydrogen being preferred.
It can further be advantageous if the exit velocity of the
reaction mixture from the mixing chamber to the reaction
space is 10 to 80 m/s.
The vapours of the silicon chloride and of the titanium
chloride can also be taken to the mixing chamber, in mixed
or separate form, by means of a carrier gas.
The required substances combustible gas, primary air and/or
secondary air can be introduced in preheated form. A
suitable temperature range is 50 to 400°C.

Furthermore, primary and/or secondary air can be enriched
with oxygen.
Preferably, the process according to the invention can be
carried out such that SiCl4 is employed as silicon halide,
TiCl4 is employed as titanium halide and the adiabatic flame
temperature Tad = 1050 ± 50°C.
A further subject of the invention is a dispersion which
comprises the silicon-titanium mixed oxide powder according
to the invention and water.
The average aggregate diameter of the silicon-titanium
mixed oxide particles in the dispersion is preferably less
than 200 nm and particularly preferably less than 100 nm.
Preferably, the following is true for the dispersion
according to the invention: 10 silicon-titanium mixed oxide the range is 12 mixed oxide Furthermore, a dispersion can be preferred which
additionally contains a basic, quaternary ammonium
compound. Dispersions are particularly preferred which
contain tetraalkylammonium hydroxides such as, for example,
tetraethylammonium hydroxide, tetra-n-propylammonium
hydroxide and/or tetra-n-butylammonium hydroxide.
The content of quaternary, basic ammonium compound in the
dispersion according to the invention is not limited. If
the dispersion is to be stored for a relatively long time,
it can be advantageous to add to it only a part of the
amount of the dispersion necessary for the preparation of a
titanium-containing zeolite. Preferably, the quaternary,
basic ammonium compound can be added in such an amount that
a pH of 9 to 11, in particular 9.5 to 10.5, results. The
dispersion shows good stability in this pH range.

If the dispersion is to be employed, for example,
immediately after its preparation for the preparation of a
titanium-containing zeolite, the dispersion can already
also contain the total amount of quaternary, basic ammonium
compound. Preferably, the following is then true: 0.12 mol of ammonium compound/mol of silicon-titanium mixed
oxide silicon-titanium mixed oxide preferred.
A further subject of the invention is a process for the
preparation of the dispersion according to the invention,
comprising the steps:
- water, which, if the silicon-titanium mixed oxide powder
introduced later leads to a pH of the aqueous phase of
4, is adjusted by addition of acids or bases to
pHs of 2 to 4, is recycled from a receiver by means of a
rotor/stator machine, and
- an amount of the silicon-titanium mixed oxide powder
according to the invention is introduced continuously or
batchwise by means of a filling device and with the
rotor/stator machine running into the shear zone between
the slots of the rotor teeth and of the stator slots
such that a predispersion having a solids content of 20
to 40% by weight results, and
- after all the silicon-titanium mixed oxide powder has
been added, the filling device is closed and the
predispersion is sheared further such that the shear
rate lies in the range between 10 000 and 40 000 s-1, and
- if appropriate water and a basic, quaternary ammonium
compound are subsequently added with retention of the
dispersion conditions.
A further subject of the invention is a process for the
preparation of a titanium-containing zeolite, in which the

silicon-titanium mixed oxide powder according to the
invention and a basic, quaternary ammonium compound are
treated in an aqueous medium at a temperature of 150 to
220°C for a period of less than 12 hours.
Preferably, the process is carried out such that the
following is true: 10 titanium mixed oxide range is 12 oxide It is furthermore advantageous to carry out the process
such that the following is true: 0.12 compound/mol of silicon-titanium mixed oxide Particularly preferably, the range is 0.13 ammonium compound/mol of silicon-titanium mixed oxide
As basic, quaternary ammonium compounds, tetraalkylammonium
hydroxides such as, for example, tetraethylammonium
hydroxide, tetra-n-propylammonium hydroxide and/or tetra-n-
butylammonium hydroxide are particularly preferred.
Basic, quaternary ammonium compounds are used as templates
which determine the crystal structure by incorporation into
the crystal lattice. Tetra-n-propylammonium hydroxide is
preferably employed for the preparation of titanium
silicalite-1 (MFI structure), tetra-n-butylammonium
hydroxide for the preparation of titanium silicalite-2 (MEL
structure) and tetraethylammonium hydroxide for the
preparation of titanium (3-zeolites (BEA crystal structure) .
A further subject of the invention is a process for the
preparation of a titanium-containing zeolite, in which the
dispersion according to the invention, if appropriate with
further addition of a basic, quaternary ammonium compound,
is treated at a temperature of 150 to 220 °C for a period of
less than 12 hours.

Under the specified conditions of the process according to
the invention, the crystallization time is conventionally
less than 12 hours. The crystals are separated by
filtering, centrifuging or decanting and washed with a
suitable washing liquid, preferably water. The crystals
are then dried if needed and calcined at a temperature
between 400°C and 1000°C, preferably between 500°C and
750°C in order to remove the template.
The particle fineness of less than 200 nm in the dispersion
leads to rapid dissolution of the particles and formation
of the titanium-containing zeolite.
A further subject of the invention is a titanium-containing
zeolite which is obtainable by the process according to the
invention starting from silicon-titanium mixed oxide
powder.
A further subject of the invention is a titanium-containing
zeolite which is obtainable by the process according to the
invention starting from the dispersion comprising silicon-
titanium mixed oxide powder.
Both titanium-containing zeolites are obtained in powder
form. For their use as an oxidation catalyst, they are
converted if needed to a form suitable for use, e.g. to
micropellets, spheres, tablets, solid cylinders, hollow
cylinders or honeycombs, using known methods for the
creation of pulverulent catalysts, such as, for example,
pelletization, spray drying, spray pelletization or
extrusion.
The titanium-containing zeolites according to the
invention can be used as catalysts in oxidation reactions
with hydrogen peroxide. In particular, they can be used as
catalysts in the epoxidation of olefins with the aid of
aqueous hydrogen peroxide in a water-miscible solvent.

Examples:
Required materials: The required materials silicon
tetrachloride and titanium tetrachloride of Examples 1 to 5
have contents of Na, K, Fe, Co, Ni, Al, Ca and Zn of
Examples 1 to 4: Titanium-silicon mixed oxide powder
according to invention
Example 1: 5.15 kg/h of silicon tetrachloride and 0.15 kg/h
of titanium tetrachloride are evaporated. The vapours are
taken to a mixing chamber by means of 15 Nm3/h of nitrogen
as a carrier gas. Separately therefrom, 2 Nm3/h of hydrogen
and 8 Nm3/h of primary air are introduced into the mixing
chamber. The reaction mixture is fed to a burner and
ignited in a central tube. The flame burns here in a water-
cooled flame tube. 15 Nm3/h of secondary air are
additionally introduced into the reaction space. The
resulting powder is separated in a filter connected in
series and subsequently treated with water vapour at 520°C
in countercurrent.
Examples 2-4 are carried out analogously to Example 1 using
the amounts listed in the table.
Example 5 is a comparative example whose composition lies
in the range claimed, but has a markedly lower BET surface
area than the claimed powders.
The substance parameters of the powders obtained are
summarized in the table.
In all examples, the content of Na is Fe £1 ppm, Co

Example 6: Preparation of a dispersion (according to the
invention)
32.5 kg of completely demineralized water are initially
introduced into a 100 1 stainless steel make-up vessel.
Subsequently, with the aid of the suction nozzle of the
Ystral Conti-TDS 4 (stator slots: 6 mm ring and 1 mm ring,
rotor/stator distance about 1 mm), 17.5 kg of the silicon-
titanium mixed oxide powder from Example 1 are drawn in
under shear conditions. After completion of the drawing-in,
the suction nozzle is closed and the 35 per cent by weight
pre-dispersion is subsequently additionally sheared at 3000
rpm for 10 min. Undesired warming of the dispersion due to
the high energy input is countered by a heat exchanger and
the temperature increase is restricted to a maximum of
40°C. Due to the acidic character of the pyrogenically
prepared silicon-titanium mixed oxide powder, the pH of the
dispersion is about 3.6.

WE CLAIM:
1. Process for the preparation of a pyrogenic silicon-titanium mixed oxide powder
having a BET surface area is 200 to 400 m2 /g, silicon dioxide content of 97.0 ±
1.5% by weight, titanium dioxide content of 3.5 + 1.0% by weight and the sum of
silicon dioxide content and titanium dioxide content being greater than 99.7% by
weight, all percentages by weight relating to the total amount of the powder, said
process is characterized in that
- 97.0 ±1.5 parts by weight calculated as SiO2 of silicon halide and 3.5 ±
1.5 parts by weight calculated as TIO2 of titanium halide are evaporated,
the vapours are taken to a mixing chamber,
- hydrogen and primary air are taken to the mixing chamber separately
therefrom,
- the mixture of the vapours of silicon halide and titanium halide, hydrogen-
containing combustible gas and primary air is subsequently ignited in a
burner and the flame is burned into a reaction chamber,
- secondary air is additionally introduced into the reaction chamber, the
solid is subsequently separated from gaseous substances, and
- the solid is subsequently freed as far as possible from halide-containing
substances by treatment with steam at temperatures of 250 to 700°C

- the amount of the required substances consisting of silicon chloride,
titanium chloride, combustible gas, primary air and secondary air being
chosen such that an adiabatic flame temperature Tad results, for which the
following is true: 900°C required substances + sum of the reaction enthalpies of the partial
reactionslhead capacity of the substances which leave the reaction
chamber, comprising silicon dioxide, water, hydrogen chloride, if
appropriate carbon dioxide, oxygen, nitrogen, and if appropriate of the
carrier gas if this is not air or nitrogen, the specific heat capacity of these
substances at 1000°C being used as a basis.
2. Process as claimed in claim 1, wherein SiCl4 is employed as silicon halide, TiCl4
is employed as titanium halide and Tad = 1050 ± 50°C.
3. Process as claimed in claim 1 or 2, wherein the exit velocity VB of the gases
employed from the burner into the reaction space is 10 to 80 m/s.

4. Process for the preparation of a dispersion comprising pyrogenic silicon-titanium
mixed oxide powder having a BET surface area is 200 to 400 m2/g, silicon
dioxide content of 97.0 ± 1.5% by weight, titanium dioxide content of 3.5 ± 1.0%
by weight and the sum of silicon dioxide content and titanium dioxide content
being greater than 99.7% by weight, all percentages by weight relating to the
total amount of the powder, comprising the steps:
- water, which, if the silicon-titanium mixed oxide powder introduced later
leads to a pH of the aqueous phase of 4, is adjusted by addition of
acids or bases to pHs of 2 to 4, is recycled from a receiver by means of a
rotor/stator machine, and 1 an amount of said silicon-titanium mixed oxide
powder is introduced continuously or batchwise by means of a filling
device and with the rotor /stator machine running into the shear zone
between the slots of the rotor teeth and of the stator slots such that a pre-
dispersion having a solids content of 20 to 40% by weight results, and
- after all the silicon-titanium mixed oxide powder has been added, the
filling device is closed and the predispersion is sheared further such that
the shear rate lies in the range between 10 000 and 40 000 s-1, and
- if appropriate water and a basic, quaternary ammonium compound are
subsequently added with retention of the dispersion conditions.


ABSTRACT

Title: A process for the preparation of pyrogenic silicon-titanium mixed oxide powder.
Process for the preparation of a pyrogenic silicon-titanium mixed oxide powder having a
BET surface area is 200 to 400 m2 /g, silicon dioxide content of 97.0 ± 1.5% by weight,
titanium dioxide content of 3.5 ± 1.0% by weight and the sum of silicon dioxide content
and titanium dioxide content being greater than 99.7% by weight, all percentages by
weight relating to the total amount of the powder, said process is characterized in that
97.0 ±1.5 parts by weight calculated as SiO2 of silicon halide and 3.5 ±1.5 parts by
weight calculated as TiO2 of titanium halide are evaporated, the vapours are taken to a
mixing chamber, hydrogen and primary air are taken to the mixing chamber separately
therefrom, the mixture of the vapours of silicon halide and titanium halide, hydrogen-
containing combustible gas and primary air is subsequently ignited in a burner and the
flame is burned into a reaction chamber, secondary air is additionally introduced into the
reaction chamber, the solid is subsequently separated from gaseous substances, and the
solid is subsequently freed as far as possible from halide-containing substances by
treatment with steam at temperatures of 250 to 700°C the amount of the required
substances consisting of silicon chloride, titanium chloride, combustible gas, primary air
and secondary air being chosen such that an adiabatic flame temperature Tad results, for
which the following is true: 900°C substances + sum of the reaction enthalpies of the partial reactionslhead capacity of the
substances which leave the reaction chamber, comprising silicon dioxide, water,
hydrogen chloride, if appropriate carbon dioxide, oxygen, nitrogen, and if appropriate of
the carrier gas if this is not air or nitrogen, the specific heat capacity of these substances
at 1000°C being used as a basis.

Documents:

4194-KOLNP-2008-(15-09-2011)-EXAMINATION REPORT REPLY RECIEVED.PDF

4194-KOLNP-2008-(15-09-2011)-OTHERS.pdf

4194-KOLNP-2008-(21-08-2012)-CORRESPONDENCE.pdf

4194-KOLNP-2008-(24-02-2012)-CORRESPONDENCE.pdf

4194-KOLNP-2008-(24-02-2012)-FORM-3.pdf

4194-KOLNP-2008-(25-04-2012)-ABSTRACT.pdf

4194-KOLNP-2008-(25-04-2012)-AMANDED CLAIMS.pdf

4194-KOLNP-2008-(25-04-2012)-CORRESPONDENCE.pdf

4194-KOLNP-2008-(25-04-2012)-DESCRIPTION (COMPLETE).pdf

4194-KOLNP-2008-(25-04-2012)-FORM-1.pdf

4194-KOLNP-2008-(25-04-2012)-FORM-2.pdf

4194-KOLNP-2008-(25-04-2012)-OTHERS.pdf

4194-kolnp-2008-abstract.pdf

4194-kolnp-2008-claims.pdf

4194-KOLNP-2008-CORRESPONDENCE 1.3.pdf

4194-KOLNP-2008-CORRESPONDENCE-1.1.pdf

4194-KOLNP-2008-CORRESPONDENCE-1.2.pdf

4194-kolnp-2008-correspondence.pdf

4194-kolnp-2008-description (complete).pdf

4194-KOLNP-2008-EXAMINATION REPORT.pdf

4194-kolnp-2008-form 1.pdf

4194-kolnp-2008-form 18.pdf

4194-kolnp-2008-form 2.pdf

4194-KOLNP-2008-FORM 3 1.2.pdf

4194-KOLNP-2008-FORM 3-1.1.pdf

4194-kolnp-2008-form 3.pdf

4194-KOLNP-2008-FORM 5 1.1.pdf

4194-kolnp-2008-form 5.pdf

4194-kolnp-2008-gpa.pdf

4194-KOLNP-2008-GRANTED-ABSTRACT.pdf

4194-KOLNP-2008-GRANTED-CLAIMS.pdf

4194-KOLNP-2008-GRANTED-DESCRIPTION (COMPLETE).pdf

4194-KOLNP-2008-GRANTED-FORM 1.pdf

4194-KOLNP-2008-GRANTED-FORM 2.pdf

4194-KOLNP-2008-GRANTED-SPECIFICATION.pdf

4194-kolnp-2008-international publication.pdf

4194-KOLNP-2008-INTERNATIONAL SEARCH REPORT 1.1.pdf

4194-kolnp-2008-international search report.pdf

4194-KOLNP-2008-OTHERS 1.1.pdf

4194-KOLNP-2008-OTHERS.pdf

4194-kolnp-2008-pct priority document notification.pdf

4194-KOLNP-2008-REPLY TO EXAMINATION REPORT.pdf

4194-kolnp-2008-specification.pdf

4194-kolnp-2008-translated copy of priority document.pdf


Patent Number 253700
Indian Patent Application Number 4194/KOLNP/2008
PG Journal Number 33/2012
Publication Date 17-Aug-2012
Grant Date 14-Aug-2012
Date of Filing 15-Oct-2008
Name of Patentee EVONIK DEGUSSA GMBH.
Applicant Address RELLINGHAUSER STRASSE 1-11, 45128 ESSEN
Inventors:
# Inventor's Name Inventor's Address
1 DR. MARTIN MÖRTERS DINKELBERGSTRASSE 6 79618 RHEINFELDEN
2 DR. KAI SCHUMACHER BAHNSTR. 30 65719 HOFHEIM
3 DR. HELMUT MANGOLD IN DER GARTEL 2 63517 RODENBACH
4 DR. STEFFEN HASENZAHL HOCHSTÄDTER LANDSTRAßE 113 63454 HANAU
PCT International Classification Number C01B 33/18
PCT International Application Number PCT/EP2007/052284
PCT International Filing date 2007-03-12
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 10 2006 017 701.0 2006-04-15 Germany