Language selection

Search

Patent 2016285 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 2016285
(54) English Title: PRODUCTION OF SPHERICAL CERAMIC POWDERS
(54) French Title: PRODUCTION DE PARTICULES DE CERAMIQUE SPHERIQUES
Status: Expired and beyond the Period of Reversal
Bibliographic Data
(51) International Patent Classification (IPC):
  • B1J 13/00 (2006.01)
(72) Inventors :
  • LUCKEVICH, LYDIA M. (Canada)
(73) Owners :
  • BODYCOTE ORTECH INC.
(71) Applicants :
  • BODYCOTE ORTECH INC. (Canada)
(74) Agent: MARKS & CLERK
(74) Associate agent:
(45) Issued: 1998-10-20
(22) Filed Date: 1990-05-08
(41) Open to Public Inspection: 1991-02-01
Examination requested: 1992-08-10
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
8917546.7 (United Kingdom) 1989-08-01

Abstracts

English Abstract


ABSTRACT OF THE DISCLOSURE
A sol-gel method is employed to produce ceramic
oxide spheres from precursors thereto. An alkanol of
the sol precursor(s) is introduced to an immiscible
hydrophilic liquid phase to cause spheroidizing of the
sol. Moisture, which initially may be present in the
immiscible liquid or may subsequently be added, is
employed to effect hydrolysis of the precursor to oxide
form. The ceramic oxide spheres are recovered from the
liquid phase and calcined to their final form.


French Abstract

Utilisation d'une méthode sol-gel pour l'obtention de sphères d'oxyde céramique à partir de leurs précurseurs. Un alcanol du ou des précurseurs de sol est introduit dans une phase liquide hydrophile non miscible pour la sphéroïdisation du sol. L'humidité, qui peut être présente initialement dans le liquide non miscible ou qui peut être ajoutée ultérieurement, sert à hydrolyser le précurseur en oxyde. Les sphères d'oxyde céramique sont récupérées à partir de la phase liquide et calcinées pour l'obtention de la forme finale.

Claims

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


14
The embodiments of the invention in which an exclusive
property or privilege is claimed are defined as follows:
1. A method of producing ceramic spheres suitable for
calcination to ceramic powders, which comprises:
contacting an anhydrous alkanol sol of at least one ceramic
oxide precursor with liquid with which said sol is immiscible to
form spheres of said sol in said immiscible liquid, and
hydrolyzing said ceramic oxide precursor in said spheres to
form ceramic oxide spheres.
2. The method of claim 1 where said spheroidizing
step and hydrolysis step are effected sequentially.
3. The method of claim 1 wherein said spheroidizing
step and hydrolysis step are effected simultaneously.
4. The method of claim 1 comprising the further
steps of recovering said ceramic particles from said immiscible
liquid and calcining said recovered particles to form a ceramic
powder.
5. The method of claim 1 wherein said anhydrous
alkanol sol is contacted with said immiscible liquid by
introducing droplets of said sol to a continuous phase of said
immiscible liquid.
6. The method of claim 5 wherein said droplets of sol are of
colloidal size.
7. The method of claim 5 wherein said immiscible
liquid is a hydrophilic liquid containing water and said
sol is hydrophobic, whereby such spheroidizing step and hydrolysis
step are effected simultaneously.
8. The method of claim 7 wherein said immiscible
liquid is a mixture containing mainly acetonitrile,
along with toluene, isopropanol, ethanol and water.
9. The method of claim 8 wherein said immiscible
liquid contains up to 5 wt.% of water.

10. The method of claim 1 wherein said ceramic
precursor is an alkoxide.
11. The method of claim 10 wherein said ceramic
precursor concentration ranges from an alkoxide
concentration of about 1 wt.% to about 80 wt.% of said
sol.
12. The method of claim 4 wherein said at least one
ceramic precursor comprises a mixture of aluminum
-tri-sec-butoxide and zirconium n-butoxide, thereby to
produce transformation toughened alumina ceramic
particles.
13. The method of claim 3 wherein said sol is
prepared by dispersing particles of at least one ceramic
oxide precursor of colloidal particle size in a alkanol
solvent.
14. The method of claim 13 wherein said alkanol has
a concentration of from about 20 wt.% to about 99 wt.%
of said sol.
15. The method of claim 12 wherein said alkanol
solvent further comprises an organic hydrocarbon solvent
to render the solvent highly hydrophobic.
16. The method of claim 15 wherein said alkanol
solvent comprises isobutanol and toluene.
17. The method of claim 15 wherein said hydrocarbon
solvent concentration from about 12 wt.% to about 40
wt.% of said sol.

Description

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


201628~
4250-1/2 88-374 MIS/CJL 1990 05 07 D4
TITLE OF INVENTION
PRODUCTION OF SPHERICAL ~ERAMIC POWDE~S
FIELD OF THE INVENTION
The present invention is directed to the production
of ceramic spheres using a sol-gel method. More
particularly the present invention is directed towards
the production of high performance ceramic powder
spheres by way of sol-gel synthetic methods using
polymerized alkoxides or similar ceramic precursors.
BACKGROUND OF THE INVENTION
Chemical methods of ceramic powder synthesis have
been increasing in prominence in recent years because of
their potential to produce homogeneous powders with
controlled particle size and morphology. The majority
of work using polymerized alkoxides has been done not
for polycrystalline ceramics or powders but in silica or
high silica glasses for optical fibre applications.
The principle behind sol-gel synthetic methods
using polymerized alkoxides is basically a
decomposition-recomposition reaction. Metal alkoxides
(metal-organic precursors) are partially hydrolyzed or
decomposed, then are recombined by polymerization or
condensation to form a metal-oxygen-metal bond. An
example of this technology is found in the use of
aluminum isopropoxide to form alumina. Aluminum
alkoxide is added to water with stirring, and hydrolysis
begins. Typically a sol is stabilized by acid addition
and heating, the solution then is gelled and fired to
yield a solid alumina body.
SUMMARY OF THE INVENTION
In accordance with the present invention, a novel
method of producing ceramic spheres suitable for
calcination to ceramic powders is provided, which

20~2~
comprises contacting an anhydrous alkanol sol of at
least one ceramic oxide precursor with liquid with which
said sol is immiscible to form spheres of said sol in
said immiscible liquid.
In accordance with an aspect of the present
invention a novel method of producing ceramic spheres is
provided wherein an anhydrous alkanol-based hydrophobic
sol containing at least one ceramic oxide precursor is
contacted with a liquid with which the sol is immiscible
to form spheres of the sol in the immiscible fluid. The
ceramic oxide precursor then is hydrolyzed to form
ceramic oxide spheres resulting in an amorphous powder
with spherical morphology. The ceramic spheres so
produced are recovered from the liquid, by filtration or
other suitable method, and calcined to form a final
ceramic powder.
The spheroidizing and hydrolyzing steps preferably
are effected simultaneously employing an immiscible
hydrophilic spheroidizing medium. Alternatively, the
spheroidizing and hydrolyzing steps may be effected
sequentially.
The present invention permits the preparation of
spherical particles of any size ranging from sub-micron
size to large spherical particles (> 1 mm) out of
structural ceramics and the application of this
technology to the synthesis of hollow spheres from
electronic or functional ceramic materials. The latter
materials may be used as piezoelectric materials for
transducer and/or sonar applications.
BRIEF DESCRIPTION OF DRAWINGS
Figure 1 is a schematic illustration of a
spheroidizing/polymerization process for forming
ceramic spheres in accordance with one embodiment of
the invention;

2~2~
Figure 2 is a schematic flow sheet for a process
for forming ceramic spheres in accordance with one
embodiment of the invention;
Figure 3 is a scanning electron photomicrograph
(SEM) of a first sample of ceramic spheres produced
using the process of Figures 1 and 2;
Figure 4 is a scanning electron photomicrograph
(SEM) of a second sample of ceramic spheres produced
using the process of Figures 1 and 2;
Figure 5 is a scanning electron photomicrograph
(SEM) of a third sample of ceramic spheres using the
process of Figures 1 and 2;
Figure 6 is a scanning electron photomicrograph
(SEM) of a fourth sample of ceramic spheres using the
process of Figures 1 and 2;
Figure 7 is a scanning electron photomicrograph
(SEM) of a fifth sample of ceramic spheres using the
process of Figures 1 and 2.
Figure 8 is a scanning electron photomicrograph
(SEM) of a sixth sample of ceramic spheres using the
process of Figures 1 and 2.
GENERAL DESCRIPTION OF INVENTION
In the present invention, ceramic oxide spheres are
formed from an anhydrous alkanol-based hydrophobic sol
containing at least one ceramic oxide precursor and
often a mixture of such precursors. For example, for
producing transformation toughened alumina, a mixture of
aluminum-tri-sec-butoxide and zirconium n-butoxide may
be employed. The ceramic oxide precursor may be any
suitable precursor which, when moistened, produces the
ceramic oxide. Alkoxides are the preferred precursors.
Two main considerations were focussed upon in
developing the preferred embodiments of the present
invention:

20~628~
(1) the sol is stable for a prolonged period (up
to many months); and
(2) the powder preparation method should use
properties of the solvents and liquids
5employed to promote the production of
spherical particles.
The first consideration was addressed by making the
sol anhydrous and hydrophobic thereby limiting the
hydrolysis of the ceramic precursor upon storage.
10The second consideration was addressed by using the
property of immiscible liquids, i.e. emulsions. In such
systems, energy is minimized by minimizing the contact
area between immiscible liquids. A spherical particle
or droplet is the morphology at which the surface area
15to volume ratio is at a minimum, thus minimizing the
contact area between the two liquids and consequently
the energy of the system.
The properties of ceramic oxide particles in
accordance with a preferred embodiment of the invention
20is shown in the schematic illustration of Figure 1 and
the process flow sheet of Figure 2.
Generally, in the sol preparation stage, the sol is
prepared by dispersing particles of the ceramic oxide
precursor of colloidal particle size in the hydrophobic
25solvent. The solvent comprises at least one alkanol,
for example, isobutanol, generally along with an organic
hydrocarbon solvent, such as toluene, to render the
solvent highly hydrophobic. The sol is maintained
anhydrous until spheroidizing is effected.
30An important aspect of the present invention is
that the moisture content in the sols is maintained low
until ceramic oxide particles are to be formed from the
sol, to minimize hydrolysis of the ceramlc oxide
precursors. To achieve this result, a dehydrating
35molecular sieve or other suitable desiccant may be added

2~235
to maintain a low moisture content in the sol,
particularly where long term storage is desirable.
The concentration of ceramic precursor in the sol
may vary widely. Successful sphere formation may be
achieved at an alkoxide concentration from about 1 to
about 80 wt.%. The spheres tend to increase in size and
decrease in number as the concentration of precursor
increases.
The concentration of alkanol present in the sol
also may vary widely. Successful sphere formation may
be achieved at a concentration of about 20 to about ~9
wt.%. The spheres tend to decrease in size and increase
in number as the concentration of alkanol increases.
The hydrophobic solvent component of the sol also
may vary widely in concentration. Spheres may be formed
at concentrations from about 12 to about 40 wt.%. The
spheres tend to increase in size and decrease in number
as the concentration of hydrophobic solvent increases.
In the powder preparation step, the sol is reacted
with a liquid in which the sol is immiscible and which
is hydrophilic. To effect such reaction, the sol is
most conveniently introduced in droplet form, to a
continuous phase of the immiscible hydrophilic liquid,
as illustrated in Figure 1, whereby the immiscible
liquid provides a spheroidizing effect on the sol
droplet. The metal alkoxide in the sol droplets is
partially hydrolyzed by water present in the hydrophilic
liquid and the hydrolysis product then recombines by
polymerization or condensation to form a metal-oxygen-
metal bond in ceramic oxide particles which result.
The spheroidizing hydrophilic liquid is a liquid
immiscible with the liquid phase of the sol and contains
water. Sphere formation has been found to be
independent of water concentration in the immiscible
liquid. The rate of hydrolysis and the physical
stability of the spheres, however, tend to depend on

20162~
water concentration. Generally, the aqueous component
may comprise less than ~ to about 5 wt.% of immiscible
liquid.
The combination of the hydrophobic nature of the
sol, the immiscibility of the liquids and the presence
of water in the hydrophilic liquid ensures that fine
powder particles of ceramic are formed.
In a modification to the above described process,
the spheroidizing and hydrolysis may be effected
sequentially rather than simultaneously. In this
modification, the sol also may be introduced initially
into dry immiscible liquid, which effects the
spheroidizing and yields unreacted spherical droplets of
sol. These droplets then are contacted with water, such
as by introducing water to the immiscible liquid,
ceramic precursor in the spheres of sol hydrolyses and
the droplet/liquid interface rigidizes. This
modification has the advantage of decreasing the volumes
of non-alkoxide components required to prepare the
powders.
Common mixed oxide ceramics used for structural
applications include al~mina, Transformation Toughened
Alumina (TTA), Partially Stabilized Zirconia (PSZ),
mullite, cordierite and spinel. Any of these materials
may be formed from suitable alkoxide precursors prepared
in accordance with the process of the present invention.
It is appreciated that the present invention has a
number of useful applications, including its suitability
for space (zero gravity) production of high performance
ceramic ball bearings. The stability of the anhydrous
sol prior to reaction with a suitable polymerizing agent
is advantageous in these applications.
DESCRIPTION OF PREFERRED EMBODIMENT
In one preferred embodiment, Transformation
Toughened Alumina (TTA) was synthesized, details of such

20~ ~2~
synthesis appearing in the Examples below. TTA is
alumina dosed with zirconia as a toughening agent.
There are two main steps involved in making the
precursors for TTA, the first being synthesis of a
stable sol containing the precursors required (sol
preparation stage), and the second being preparation of
a powder through reaction of this sol with the liquid
(powder preparation stage). TTA is then prepared by
heat treatment of the powder formed.
TTA, like other common mixed oxide ceramics for use
in structural applications, uses ceramic precursor
alkoxides which are highly reactive and to-date have
resulted in sols with high moisture sensitivity. As
such, the reactions have been difficult to control. The
anhydrous sols of the present invention overcome this
problem and permit the development of a reliable
reproducible method for the production of ceramic oxide
structural spheres of TTA. The anhydrous sols of the
present invention not only enhance the reliability and
reproducibility of the sol-gel methodology employed
herein but are also stable for long periods of time (on
the order of months).
In a preferred embodiment for the preparation of
TTA, the sol components are aluminum-tri-sec-butoxide,
zirconium-n-butoxide, isobutanol and toluene. The
amount of each alkoxide is selected to yield an
A12O3:ZrO2 ratio of about 9:1. This corresponds with
the mid-range of ratios commonly used in TTA synthesis
via conventional dry mixing routes. The isobutanol
concentration was selected to be the lowest which
yielded intact spherical particles, namely about 45 wt.%
isobutanol in the sol. The toluene concentration, also
was the lowest which yielded mainly intact spherical
particles, namely about 17 wt.%. It is desirable to
have the sol as concentrated as possible to minimize
solvent evaporation and particle shrinkage.

'~0~ ~2~
In this preferred embodiment for the preparation of
TTA, the dry alcohol/toluene-based sol was added to an
immiscible wet solvent, namely SPHEROL
SPHEROL is a trade mark for a proprietary mixture
containing mainly acetonitrile, along with toluene
isopropanol, ethanol and water. In this preferred
embodiment, it was noted that the addition of toluene to
the sol to make it strongly hydrophobic is an important
aspect of this invention. The strongly hydrophobic
nature of the toluene combined with keeping the sol dry
allowed for a highly reactive and successful formation
of ceramic particles during the powder preparation
stage. As shown in the SEM photographs in Figures 3
and 4, micron and sub-micron sized spheres were
produced. The ratio of sol to spheroidizing liquid is
best kept to a minimum to maintain total volumes, cost
and solvent recovery systems at a minimum. For the
formation of TTA, a volume ratio of 10:1 (SP~EROL to
sol~ is preferred.
Toluene is extremely non-polar and is an important
component in making toughened alumina spheres. Toluene
makes the sol less polar and enhances sphere formation
in the TTA system. The usefulness of toluene to enhance
sphere formation and/or size depends on the ceramic
precursors used.
Other ceramics, in addition to Transformation
Toughened Alumina (TTA), have potential application as
structural ceramics. These include mullite
(3A1203 2SiO2), cordierite (xMgO yA12o3 zsio2) and
spinel (Mg A1203). In addition, hollow electronic
ceramic spheres have potential for use as magnetic
devices. Barium titanate (BaTiO3) is an example of an
electronic ceramic.

2Q1 ~2~~a
~PhES
Example l
This Example illustrates the use of aluminum-tri-
sec-butoxide and tetraethylorthosilicate to form
mullite ceramic particles.
Aluminum-tri-sec-butoxide was diluted with
isopropanol to form a slightly hazy mixture.
Tetraethylorthosilicate (TEOS) was diluted with dry
ethanol. A precipitate formed immediately upon addition
of the aluminum-tri-sec-butoxide mixture to the stirred
TEOS mixture. After ~ hour of stirring, the precipitate
was stored overnight, refluxed at ~86C under a nitrogen
atmosphere for about 6 hours, cooled and stored in a
stoppered flask. The resulting sol (sol number 25) was
still slightly hazy.
The powder was prepared by injecting droplets of
the sol into stirred, wet SPHEROL (150 mL). Stirring
was continued for 5 minutes. The resulting powder was
filtered, washed with acetone and dried.
Optical microscopy examination of the powder
revealed several spheres of various sizes (16 to 54~m in
diameter). SEM examination revealed large spheres and
lumps of powder at low magnifications. High
magnification showed the powder lumps consist of
tightly-packed sub-micron spheres. SEM photographs are
shown in Figuxe 5.
Example 2
This Example illustrates the preparation of ceramic
powders of cordierite (xMgO yAl2O3 zSiO2) and spinel
(MgO Al2O3). Anhydrous sols containing cordierite and
spinel precursors were provided by UES of Dayton, Ohio.
The powders were prepared by injecting sol into stirred,
wet SPHEROL. Upon completion of sol addition, the
mixture was stirred for 5 minutes. The resulting powder
was filtered, washed with acetone and dried.

~Q16~ 5
The dried powders were examined using optical
microscopy and SEM. The microscopy observations are
given in Table 1, below. SEM photographs of the
products are shown in Figures 6 and 7.

~ L~285
11
TABLE 1
PREPARATION OF CORDIERITE AND SPINEL CERAMIC POWDERS
Powder Particle Size/Morphology
Number Sol Used Observations on SEM
23-xSAM-5 tCordierite Low magnification (~lOOOX):
from UES) some spheres, fines
High magnifications (~5000X
and ~25000X): fines consist
of very small spheres; some
have irregular shape.
24-50AM-5 (Spinel Low magnification (~lOOOX~:
from UES) few large spheres; fines on
large spheres.
High magnifications (~5000X
and ~25000X): fines consist
of small spheres; many
spheres have irregular
shape.

201628~
12
The powders produced were examined using energy
dispersive x-ray analysis (EDXA) to determine the atomic
percentages of their elemental components. In order to
form the desired crystal structures upon calcination,
the amorphous powders must contain the required ratios
of metallic elements. EDXA results and elemental
requirements are given in following Tables 2 and 3.
TABLE 2
EDXA RESULTS AND ELEMENTAL REOUIREMENT
FOR POWDER NUMBER: 23-xSAM-5. CORDIERITE
TrialElements Required* Elements Found
Number(atomic percent) (atomic percent~
Si Al Mq Si Al Mq Cu Cl
1~5.5 36.4 18.2 42.20 49.12 8.320.35
2 41.42 49.04 8.441.10
3 41.95 48.50 7.900.68 0.97
*for most favoured composition
TABLE 3
EDXA RESULTS AND ELEMEi~AL REOUIREMENTS
FOR POWDER NUMBER: 24-50AM-5, SPINEL
Trial Elements Required Elements Found
Number(atomic percentl (atomic percent)
Al Ma Al Mq Cu Si Cl Ba
1 66.67 33~33 84.09 15.21 0.70
2 81.18 14.30 2.192.00 0.32
3 83.21 13.09 2.701.00
4 77.39 15.82 6O79

20~28~
Example 3
Transformation toughened alumina (TTA) was
prepared using zirconia as a toughening agent. The sol
had the following composition:
isobutanol 34.8 wt%
zirconium n-butoxide 3.8 wt%
aluminum-tri-sec-butoxide 39.7 wt%
toluene 21.7 wt%
The amount of each alkoxide was selected to yield a mole
ratio AL2O3:ZrO2 of 9:1. The sol was kept dry by
continuous contact with a Type 4A Molecular Sieve.
Anhydrous sol was introduced into SPHEROL. The
sol: SPHEROL ratio was 1:10. Spheres of different sizes
were yielded including many sub-micron spheres as seen
in the SEM photograph of Figure 8.
SUMMARY OF DISCLOSURE
In summary of this disclosure, the present
invention provides a novel method of producing ceramic
spheres employing a sol-gel method, in which an
anhydrous hydrophobic sol of ceramic oxide precursors is
introduced to an immisaible hydrophilic liquid to form
spheres, which then are calcined to the final ceramic
sphere. Although preferred embodiments of the
invention have been described herein in detail, it will
be understood by those skilled in the art that
variations may be made thereto without departing from
the spirit of the invention or the scope of the appended
claims.

Representative Drawing
A single figure which represents the drawing illustrating the invention.
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
Time Limit for Reversal Expired 2002-05-08
Letter Sent 2001-05-08
Letter Sent 2000-06-22
Inactive: Office letter 1999-07-16
Inactive: Late MF processed 1999-05-11
Inactive: Multiple transfers 1999-05-05
Grant by Issuance 1998-10-20
Pre-grant 1998-06-02
Inactive: Final fee received 1998-06-02
Notice of Allowance is Issued 1998-04-16
Notice of Allowance is Issued 1998-04-16
4 1998-04-16
Letter Sent 1998-04-16
Amendment Received - Voluntary Amendment 1998-03-19
Inactive: IPC removed 1998-03-16
Inactive: First IPC assigned 1998-03-16
Inactive: IPC assigned 1998-03-16
Inactive: Approved for allowance (AFA) 1998-03-16
Inactive: S.30(2) Rules - Examiner requisition 1998-02-20
Amendment Received - Voluntary Amendment 1998-02-02
Inactive: Application prosecuted on TS as of Log entry date 1997-08-26
Inactive: Status info is complete as of Log entry date 1997-08-26
All Requirements for Examination Determined Compliant 1992-08-10
Request for Examination Requirements Determined Compliant 1992-08-10
Application Published (Open to Public Inspection) 1991-02-01

Abandonment History

There is no abandonment history.

Maintenance Fee

The last payment was received on 1998-01-28

Note : If the full payment has not been received on or before the date indicated, a further fee may be required which may be one of the following

  • the reinstatement fee;
  • the late payment fee; or
  • additional fee to reverse deemed expiry.

Patent fees are adjusted on the 1st of January every year. The amounts above are the current amounts if received by December 31 of the current year.
Please refer to the CIPO Patent Fees web page to see all current fee amounts.

Fee History

Fee Type Anniversary Year Due Date Paid Date
Registration of a document 1990-05-08
Registration of a document 1991-05-15
Request for examination - standard 1992-08-10
MF (application, 8th anniv.) - standard 08 1998-05-08 1998-01-28
Final fee - standard 1998-06-02
Registration of a document 1999-05-05
Reversal of deemed expiry 1999-05-10 1999-05-11
MF (patent, 9th anniv.) - standard 1999-05-10 1999-05-11
MF (patent, 10th anniv.) - standard 2000-05-08 2000-05-08
Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
BODYCOTE ORTECH INC.
Past Owners on Record
LYDIA M. LUCKEVICH
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 (Temporarily unavailable). 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 1998-02-01 2 64
Cover Page 1998-09-08 1 44
Drawings 1994-04-09 9 320
Claims 1994-04-09 2 60
Description 1994-04-09 13 411
Cover Page 1994-04-09 1 12
Abstract 1994-04-09 1 12
Representative drawing 1998-09-08 1 12
Commissioner's Notice - Application Found Allowable 1998-04-15 1 164
Late Payment Acknowledgement 1999-05-24 1 172
Maintenance Fee Notice 2001-06-04 1 178
Maintenance Fee Notice 2001-06-04 1 178
Correspondence 1998-06-01 1 55
Fees 1998-01-27 1 55
Fees 1999-05-10 2 63
Fees 2000-05-07 1 53
Correspondence 1999-07-15 1 6
Fees 1997-02-09 1 55
Fees 1996-01-11 1 33
Fees 1995-01-24 1 40
Fees 1994-01-16 1 28
Fees 1993-02-10 1 28
Fees 1992-03-25 1 29