Language selection

Search

Patent 1142905 Summary

Third-party information liability

Some of the information on this Web page has been provided by external sources. The Government of Canada is not responsible for the accuracy, reliability or currency of the information supplied by external sources. Users wishing to rely upon this information should consult directly with the source of the information. Content provided by external sources is not subject to official languages, privacy and accessibility requirements.

Claims and Abstract availability

Any discrepancies in the text and image of the Claims and Abstract are due to differing posting times. Text of the Claims and Abstract are posted:

  • At the time the application is open to public inspection;
  • At the time of issue of the patent (grant).
(12) Patent: (11) CA 1142905
(21) Application Number: 1142905
(54) English Title: PREPARATION OF A BORO-ALUMINO-SILICATE ZEOLITE OF THE ZSM-5 STRUCTURAL TYPE
(54) French Title: PREPARATION D'UN ZEOLITE BORO-ALUMINO-SILICATE DE TYPE STRUCTUREL ZSM-5
Status: Term Expired - Post Grant
Bibliographic Data
(51) International Patent Classification (IPC):
  • B01J 29/06 (2006.01)
  • B01J 29/40 (2006.01)
  • B01J 29/86 (2006.01)
  • C01B 39/40 (2006.01)
  • C07C 1/20 (2006.01)
(72) Inventors :
  • MAROSI, LASZLO (Germany)
  • STABENOW, JOACHIM (Germany)
  • SCHWARZMANN, MATTHIAS (Germany)
(73) Owners :
  • BASF AKTIENGESELLSCHAFT
(71) Applicants :
  • BASF AKTIENGESELLSCHAFT (Germany)
(74) Agent: ROBIC, ROBIC & ASSOCIES/ASSOCIATES
(74) Associate agent:
(45) Issued: 1983-03-15
(22) Filed Date: 1980-02-20
Availability of licence: N/A
Dedicated to the Public: N/A
(25) Language of filing: English

Patent Cooperation Treaty (PCT): No

(30) Application Priority Data:
Application No. Country/Territory Date
P 29 09 929.4 (Germany) 1979-03-14

Abstracts

English Abstract


ABSTRACT OF THE DISCLOSURE:
The present invention is directed to a process for the
preparation of a boro-alumino-silicate zeolite of the ZSM-5
structural type from SiO2, an alkali and an oxide of a trivalent
metal, by hydrothermal crystallization in the presence of an
amine, wherein finely ground low-alkali borosilicate glasses are
used as the starting material. The crystallization is preferably
carried out in the presence of hexamethylenediamine.


Claims

Note: Claims are shown in the official language in which they were submitted.


The embodiments of the invention in which an
exclusive property or privilege is claimed are defined
as follows:
1. Boro-alumino-silicate zeolite of the ZSM-5
structural type.
2. A process for the preparation of a boro-alumino-
silicate zeolite of the ZSM-5 structural type from SiO2,
an alkali and an oxide of a trivalent metal, by hydro-
thermal crystallization in the presence of an amine,
wherein finely ground low-alkali borosilicate glasses
are used as the starting material.
3. A process as claimed in claim 2, wherein
the crystallization is carried out in the presence of
a diamine.
4. A process as claimed in claim 3, wherein
hexamethylenediamine is used.
5. A process as claimed in claim 2, 3 or 4,
wherein the solids content in the reaction mixture is
greater than 25% by weight.
6. Method for conversion of lower alcohols
and/or dialkyl ethers to hydrocarbons which contain
aromatics and/or to olefins, wherein use is made of the
zeolites as prepared by a process as claimed in claim 2.

Description

Note: Descriptions are shown in the official language in which they were submitted.


~z~s
The preparation of zeolites of the ZSM-5 type
from reaction mixtures which contain SiO2, ~12O3 and
an alkali, under hydrothermal conditions in the
presence of an amine, has been disclosed. SiO2-
containing starting materials are in particular water-
glass, various silicas and silicic acid sols.
Because of the low space-time yield, these
processes are expensive, since the solids content o~
the reaction mixtures is only about 10% by weight.
The crystallizatio~ requires about 5 days.
We have ~ound that in the preparation of a
boro-alumino-silicate zeolite of the ZSM-5 structural
type from SiO2, an alkali and an oxide of a trivalent
metal, by hydrothermal crystallization in the presence
of an amine, a substantial simplification of the
process and improvement of the space-time yield is
achieved if finely ground low-alkali borosilicate
glasses are used as the starting material~
~dvantageously, the process according to the
inv~nkion ia carried out in the presence of a diamine,
especially hexamethylenediamine.
It is surprising~tha-t reaction mixtures with
solids contents of more than 25% by weight can be
crystallized if the reackion is carried out in the
presence of a diamine and a finely ground glass powder
is used as the starting material. Compared to
pyrogenic silica, silicic acid sols or waterglass,
glass is regarded as a relatively inert material. It
was surprising thak glass could be con-

ll~Z~1~5
.
-2- o.z. 0050/033722
verted at all using diamines, which are only weakly
basic, and that using this method the space-time yield
~uldevenbe increased substantially
The process according to the invention can be
: carried out by mixing ~inely ground glass powder with an
aqueous solution o~ an organic diamine, the solids con-
. . tent ad~antageously being more than 25% ~y weight, and
then heating the mixture for from 1 to 10 days at from
100 to 200C under its autogenous pressure, whilst
stirring or shakin~, until crystallization occurs.
The.crystals are separated from the mother liquor, washed
~nd dried Preferably, the process is carried out at
from 140 to 160C 9 with a reaction time of from 2 to 6
days.
The starting materials used are amines, advan-
tageously diamines, for example hexamethylenediamine,
in aqueous solution. Various t~pes oX glass may be
used. Finely ground low-alkali borosilicate glasses
are particularly suitable. In that case, zeolites
which are o~ the boro-alumino-3ilicate type and which
exhibit the crystal structure of the convention~l ZSM-5
aluminosilicate zeolite are obtained.
The zeolites prepared according to the inventicn
contain SiO2 and A1203~ and where appropriate B203, in
various ratios depending on the composition of the
glass used; for example, they may contain SiO2 and
A1203 in a molar ratio or f rom 30:1 to 200:1,
~nd S102 and 323 in a molar ratio of from 3:1 to

2~115
- ~ - o.Z~ C050/033722
200:1, Dependin~ on the type of glass used7 other com-
ponents may also be present in the zeolite. Sub-
stantial amounts of the amine used may also be accommo-
dated in the inter-crystalline pores, This amine
can be removed from the pores by, ~or example, combustion,
whereby catalytically active materials are produced,
The zeolite may also have an alkali content which varies
depending on the composition of the glass used. The
alkali metal ions can be replaced by protons or other
cations with the aid of conventional ion exchange
techniques,
The zeolites prepared according to the invention
can be used as catalysts for the con~ersion of methanol
and/or dimethyl ether or ethanol or
diethyl ether into aromatic hydrocarbons and/or olefins,
The zeolites can furthermore be used in alkylation re-
actions and isomerization reactions,
The Example which follows illustrates the process
according to the invention,
EXAMPLE
20 . 45 g of a finely ground commercial borosilicate
glass which contains about 80~ by weight of SiO2, 12.9%
by weight of B203 , 2.27% by weight of
A1203 and 3,25% by weight of Na20 are introduced into
118 g of a 50 per cent strength aqueous hexamethylene-
diamine solution and the mixture is heated for 5 days at
150C under autogenous pressure, whilst being stirred,
The crystalline product is filtered off, washed and
dried at 100C~ According to X-ray diffraction

96~5
_ 4 _ O.Z. C050/oi3722
analysis, it consists o~ well-crystallized material of
the structural type of the co~ventional ZSM-5 alumino-
silicate zeolite.
Chemical analysis gives the following results:
5,05/0 of B203; 2.420,6 of A1203; 78.70,6 of SiO; 1,69% of
Na~0; remainder hexamethylenediamine/H20,
If, under the same reaction conditions, 60 g of
the same finely ground glass powder are employed in 118 g
of hexamethylenediamine solution9 a 100% crystallized
end product is again obtained.

Representative Drawing

Sorry, the representative drawing for patent document number 1142905 was not found.

Administrative Status

2024-08-01:As part of the Next Generation Patents (NGP) transition, the Canadian Patents Database (CPD) now contains a more detailed Event History, which replicates the Event Log of our new back-office solution.

Please note that "Inactive:" events refers to events no longer in use in our new back-office solution.

For a clearer understanding of the status of the application/patent presented on this page, the site Disclaimer , as well as the definitions for Patent , Event History , Maintenance Fee  and Payment History  should be consulted.

Event History

Description Date
Inactive: IPC from MCD 2006-03-11
Inactive: IPC from MCD 2006-03-11
Inactive: IPC from MCD 2006-03-11
Inactive: Expired (old Act Patent) latest possible expiry date 2000-03-15
Grant by Issuance 1983-03-15

Abandonment History

There is no abandonment history.

Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
BASF AKTIENGESELLSCHAFT
Past Owners on Record
JOACHIM STABENOW
LASZLO MAROSI
MATTHIAS SCHWARZMANN
Past Owners that do not appear in the "Owners on Record" listing will appear in other documentation within the application.
Documents

To view selected files, please enter reCAPTCHA code :



To view images, click a link in the Document Description column. To download the documents, select one or more checkboxes in the first column and then click the "Download Selected in PDF format (Zip Archive)" or the "Download Selected as Single PDF" button.

List of published and non-published patent-specific documents on the CPD .

If you have any difficulty accessing content, you can call the Client Service Centre at 1-866-997-1936 or send them an e-mail at CIPO Client Service Centre.


Document
Description 
Date
(yyyy-mm-dd) 
Number of pages   Size of Image (KB) 
Claims 1994-01-25 1 27
Cover Page 1994-01-25 1 19
Abstract 1994-01-25 1 13
Drawings 1994-01-25 1 12
Descriptions 1994-01-25 4 126