Language selection

Search

Patent 2268076 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 Application: (11) CA 2268076
(54) English Title: METHOD FOR PREPARING COLOURED PIGMENTS WITH TITANIUM DIOXIDE BASE
(54) French Title: PROCEDE DE PREPARATION DE PIGMENTS COLORES A BASE DE DIOXYDE DE TITANE
Status: Deemed Abandoned and Beyond the Period of Reinstatement - Pending Response to Notice of Disregarded Communication
Bibliographic Data
(51) International Patent Classification (IPC):
  • C09C 1/36 (2006.01)
  • C09C 1/00 (2006.01)
(72) Inventors :
  • CHOPIN, THIERRY (France)
  • HUGUENIN, DENIS (France)
(73) Owners :
  • MILLENNIUM INORGANIC CHEMICALS S.A.
(71) Applicants :
  • MILLENNIUM INORGANIC CHEMICALS S.A. (France)
(74) Agent: ROBIC AGENCE PI S.E.C./ROBIC IP AGENCY LP
(74) Associate agent:
(45) Issued:
(86) PCT Filing Date: 1997-09-29
(87) Open to Public Inspection: 1998-04-16
Examination requested: 2000-09-27
Availability of licence: N/A
Dedicated to the Public: N/A
(25) Language of filing: English

Patent Cooperation Treaty (PCT): Yes
(86) PCT Filing Number: PCT/FR1997/001712
(87) International Publication Number: WO 1998015599
(85) National Entry: 1999-03-30

(30) Application Priority Data:
Application No. Country/Territory Date
96/12145 (France) 1996-10-04

Abstracts

English Abstract


The invention concerns a method for preparing coloured pigments with titanium
dioxide base comprising the calcination of octahedrite dioxide until complete
transformation of the octahedrite titanium dioxide into rutile titanium
dioxide, in which is used an octahedrite titanium dioxide having a rutile
phase temperature of at least 1000 ~C and a proportion of sulphate, expressed
in SO3, of at most 1 wt. %.


French Abstract

La présente invention a pour objet un procédé pour la préparation de pigments colorés à base de dioxyde de titane comprenant la calcination de dioxyde anatase jusqu'à transformation complète du dioxyde de titane anatase en dioxyde de titane rutile, dans lequel on utilise un dioxyde de titane anatase présentant une température de rutilisation d'au moins 1000 ·C et un taux de sulfate, exprimé en SO¿3?, d'au plus 1 % en poids.

Claims

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


11
CLAIMS
1. A process for the preparation of titanium dioxide based colored pigments
including the
calcination of anatase titanium dioxide until complete transformation of the
anatase
titanium dioxide into rutile titanium dioxide, characterized in that an
anatase titanium
dioxide with a rutilization temperature of at least 1000 ~ C, preferably at
least 1060 ~ C, and
a sulfate level, expressed as SO3, of at most 1 wt.%, preferably less than
0.8%, is used.
2. The process according to Claim 1, characterized in that it is includes the
steps of:
a) mixing of said anatase titanium dioxide with at least one pigmentation
additive,
b) grinding of the resulting mixture, and
c) calcination in an oxidizing atmosphere.
3. The process according to either of Claims 1 or 2, characterized in that the
BET specific
surface of the anatase titanium dioxide is at least 250 m2/g.
4. The process according to either of Claims 2 or 3, characterized in that in
step a) the
mixing is performed dry starting with an anatase titanium dioxide powder.
5. The process according to Claim 4, characterized in that said powder is
composed of
agglomerates of titanium dioxide particles, with the average size of these
agglomerates
between 1 and 2 µm and the average size of the particles between 40 and 60
nm.
6. The process according to either of Claims 2 or 3, characterized in that in
step a) the
mixing is performed starting from an aqueous suspension of anatase titanium
dioxide,
with the water of the suspension eliminated prior to grinding the mixture.
7. The process according to Claim 6, characterized in that the aqueous
suspension
includes suspended anatase titanium dioxide particles with an average size
between 40
and 60 nm.
8. The process according to any one of Claims 2 through 7, characterized in
that said
pigmentation additive is chosen from among the compounds of the transition
elements
Sb, Cr, Ni, Co, Zn, Cu, Mn and W, which are either in the form of oxides or in
the form
of compounds oxidizable in an oxidizing atmosphere.

12
9. The process according to Claim 8, characterized in that in step a), said
anatase titanium
dioxide is mixed with compounds of antimony and chromium, with the molar ratio
of
antimony to chromium between 0.8 to 1.2, preferably equal to 1.
10. The process according to any one of Claims 2 through 9, characterized in
that
calcination occurs at a temperature between 800 and 1400 ~ C.
11. Titanium dioxide based colored pigments obtained by implementing a process
according to any one of Claims 1 to 10.
12. Use of an anatase titanium dioxide showing a rutilization temperature of
at least
1000 ~ C, preferably at least 1060 ~ C, and a sulfate level, expressed as SO3,
of at the most 1
wt.-%, preferably less than 0.8%, for the preparation of titanium dioxide
based colored
pigments.

Description

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


CA 02268076 1999-03-30
1
METHOD FOR PREPARING COLOURED PIGMENTS
WITH TITANIUM DIOXIDE BASE
The invention concerns a process for the preparation of titanium dioxide based
colored pigments. The invention also concerns the colored pigments obtained
through this
process.
Rutile phase colored pigments, i.e., composed primarily of rutile titanium
dioxide
are commonly used as coloring substances in plastic materials, paints and
varnishes and
also in the cosmetics and galenic fields.
These prior art pigments are generally prepared by (i) mixing anatase titanium
dioxide with one or a plurality of pigmentation additives, (ii) grinding then
(iii)
calcination.
These colored pigments must meet a certain number of criteria and, in
particular,
must have good stability to temperature, light, and also to decomposition by
acid or basic
chemical agents. DE 36 04 317 proposes colored pigments having improved
thermostability containing from 0.1 to 2 wt.% magnesium in addifion to a
ternary system
composed of titanium, antimony and chromium.
2 0 It is, in fact, essential that the colors of the pigments do not shade
off, for instance,
when they are added to plastic materials or paints, or when they are subj
ected to
particularly severe climatic conditions. Along the same line of thought, EP
318 783
recommends incorporation of lithium at a rate of 0.0l up to 0.25 wt.%, to
limit the
tendency toward discoloration of rutile phase pigments composed of chromium
and
antimony subjected to a quenching treatment.
However, the colorations from rutile phase pigments used in industry to date
are
not always satisfactory from the point of view of intensity of the shades and
color
saturation.
The invention proposes to resolve the problem of intensifying the shades by
providing an improved process for the preparation of titanium dioxide based
colored
pigments. The colored pigments obtained through this process offer a palette
of colors
that are more intense than those currently available on the market.

CA 02268076 1999-03-30
r=vv=.
_...
2
To that end, the invention concerns a process for the preparation of titanium
dioxide based colored pigments including the calcination of anatase titanium
dioxide until
complete transformation of the anatase titanium dioxide into rutile titanium
dioxide, in
which an anatase titanium dioxide with a rutilization temperature of at least
1000 ~ C,
preferably at least 1060 ~ C" and a sulfate level, expressed as S03, of at
most 1 wt.%,
preferably less than 0.8%,is used.
According to a first essential characteristic of the invention, the titanium
dioxide
used must have a sulfate level, expressed as S03, of at most 1 wt.%,
preferably less than
0.8%. It was noted that starting with an anatase titanium dioxide with an
excessively high
sulfate level yields a pigment shade which is not sufficiently intense. The
lowest possible
sulfate level is more advantageous.
The sulfate level is easily determined by the person skilled in the art using
any one
of the methods of analysis known in the art, for example, by x-ray
fluorescence. -
This sulfate content in the anatase titanium dioxide may be controlled during
the
manufacture of the anatase titanium dioxide.
The starting anatase titanium dioxides that may be used in the process
according
to the invention are prepared according to methods known to the person skilled
in the art.
In this regard, reference may be made to the works of Unman Band (vol. 18, p.
574) and
Kirk Othmer (vol. 23, p. 146). Preferably, the anatase titanium dioxide is
obtained in
three steps through ( 1 ) hydrolysis of a titanium sulfate solution, (2)
filtration of the
hydrolysate, and (3) washing of the filtrate with water.
The sulfate content of the titanium dioxide may be controlled, in particular,
during
the step (3) of washing of the filtrate.
According to a second essential characteristic of the invention, the titanium
dioxide used must have a rutilization temperature of at least 1000 ~ C,
preferably at least
1060~C.
Control of the rutilization temperature of a titanium dioxide is generally
performed during the synthesis of the titanium dioxide. The degree of purity
of the
anatase phase titanium dioxide may be a controlling element of this
temperature: the
closer the level of anatase titanium dioxide is to l00%, the higher the
rutilization
temperature.
This level of anatase may, in particular, be adjusted in the step (1) by
incorporation of seeds into the

CA 02268076 1999-03-30
~' v;'
~.T~.
3
hydrolysis medium. These serve to direct the nature of the hydrolysate formed:
Depending on the nature of the titanium dioxide seeds introduced, the
resulting
hydrolysate, primarily made up of anatase titanium dioxide, will include a
higher or lower
percentage of rutile titanium dioxide, with the objective being to reduce the
percentage.
Anatase titanium dioxides that have the necessary characteristics to be used
in the
process according to the invention are marketed; for example, by the Rhone
Poulenc
Company. The titanium dioxide sold by the Rhone Poulenc Company under the
reference
G5 is a powder; the Rhone Poulenc Company also supplies a titanium dioxide as
a sol
under the reference SS-300.
The rutilization temperature, which is not always indicated by the
manufacturer, is
easily determined by the person skilled in the art by implementing the
following operating
protocol,
The rutilization temperature is generally defined as being that at which 50
wt.%
of the anatase phase of an anatase titanium dioxide has been transformed into
the rutile
phase through calcination. According to the invention, the rutilization
temperature is
determined by high temperature x=ray diffractometry.
To avoid the influence of extrinsic parameters (such as the exact conditions
of the
rise in temperature), this determination takes place under very precise
operating
conditions: the anatase titanium dioxide sample is placed on a flat platinum
substrate and
kept in a confined atmosphere (without air currents) during calcination, for
example, in a
closed chamber. The temperature of the chamber is increased at the rate of 5 ~
C/min. up to
1250~C.
Diffractometry measurements are taken between 650~C and 1250~C. At regular
intervals (for example, every 5 0 ~ C), a dif&actogram is drawn, the
acquisition time being
fixed at 10 seconds over an angular range from 10 ~ to 60 ~ scanned by steps
of 0.032 ~ .
Preliminary experiments are performed in this manner with reference samples of
100% of rutile phase and 100% of anatase phase, respectively.
On the reference diffractograms obtained, the bands corresponding to the
anatase
and rutile titanium dioxides, respectively, are located.
The experiment is then performed under the same conditions with the titanium
dioxide sample to be analyzed.
By comparing the surface area of the most intense band of the two phases with
those marked on the diffractograms drawn from the reference samples, a
calculation is
made at each temperature of the proportion of rutile phase formed.

CA 02268076 1999-03-30
~'._~:i. , .;a :1,
4
The temperature at which an equal percentage of rutile phase and anatase phase
is
observed is the rutilization temperature.
According to the invention, the rutilization temperature must be at least 1000
~ C,
preferably at least 1060 ~ C. A temperature of less than 1000 ~ C is
insufficient from the
point of view of intensification of shades and of color saturation.
According to a preferred embodiment of the invention, the process includes the
following steps:
a) mixing the anatase titanium dioxide with at least one pigmentation
additive;
b) grinding the resulting mixture, and
c) calcination in an oxidizing atmosphere.
The mixing of anatase titanium dioxide with one or more pigmentation additives
may be performed dry or starting from an aqueous suspension.
To facilitate the mixing operation, selection of an anatase titanium dioxide
with a
BET specific surface of at least 250 g/m2 [sic m2/gJ is preferred. .
BET specific surface is understood to mean the specific surface measured by
the
BET method, i.e., by nitrogen adsorption, in accordance with ASTM standard
03663-78
established on the basis of the BRUNALJER-EMMETT-TELLER method described in
the periodical, "The Journal of the American Society", ,~Q, 309 (1938). When
the titanium
dioxide is in the form of an aqueous suspension (for example, a sol), the
aqueous
suspension is first atomized prior to measuring its specific surface.
When the mixing operation a) is performed dry, the anatase titanium dioxide is
in
the form of a powder composed of agglomerates of particles, with the average
size of
these agglomerates between l and 2 ~,m and the average size of the particles
between 40
and 60 nm.
Such a powder may be obtained by a prior art means, by implementing the steps
of
- hydrolysis of a titanium sulfate solution,
- filtration of the hydrolysate,
- washing of the filtrate with water,
- resuspension of the filtrate in water, and
- atomization of the resulting suspension.
According to another embodiment, the mixing a) may be performed in solution
starting from anatase titanium dioxide particles suspended in an aqueous
medium, with
the average size of the particles ranging between 40 and 60 nm. Prior to
grinding and
calcination, the water is, in this case, eliminated from the aqueous
suspension. This
second embodiment is even more advantageous insofar as it results

CA 02268076 1999-03-30
;:,
r~ ..v
in pigments that have even more intense colors, in comparison to the first
embodiment
according to which the mixing operation a) is performed dry starting from the
corresponding anatase titanium dioxide powder.
In all cases, a reduction in size of the particles facilitates the mixing
operation.
The anatase titanium dioxide based aqueous suspension may be obtained by
implementing the following steps:
- hydrolysis of a titanium sulfate solution,
- filtration of the hydrolysate,
- washing of the filtrate with water,
- redispersion of the filtrate in an acidified medium, for example, a nitric
acid or
hydrochloric acid solution. The use of sulfuric acid will be avoided at this
stage so as not
to increase the. sulfate level.
The pigmentary additives are those generally used in the art..These are
chosen, for
example, from among the compounds of the transition elements Sb, Cr, Ni, Co,
Zn, Cu,
Mn and W, and are either in the oxide form (particularly, Sb205, Cr203, NiO,
CuO, Mn0
and W03), of in the form of compounds oxidizable in an oxidizing atmosphere,
such as
that used during the calcination stage.
Preferably, a mixture of titanium dioxide and compounds of chromium and
antimony, in which the molar ratio of antimony to chromium is close to 1, for
example,
between 0.8 and 1.2, will be selected.
For informational purposes, it should be noted that calcination may take place
in
an oxygen or air atmosphere, with the calcination temperature advantageously
between
800 and l400~C.
Prior to grinding and calcination of the titanium dioxide based mixture, it is
possible to add mineral additives to it (called "mineralizers" in the art),
which are, for
example, sodium fluoride, sodium chloride, potassium chloride, calcium
fluoride or
calcium chloride. It is also possible to envisage the addition of lithium
compounds such
as those described in EP 3l8 783 (carbonate, fluoride, chloride, oxide,
hydroxide, sulfate,
nitrate, phosphate, lithium antimonate or lithium titanate) or magnesium
compounds,
such as are recommended in DE 36 04 317 (magnesium carbonate and oxide).
The invention also concerns the colored pigments obtained through the process
described above. These may be used in plastic materials, paints and varnishes,
and also in
the cosmetics and galenic fields.

CA 02268076 1999-03-30
a .:::
~x
6
And finally, the invention concerns the use of an anatase titanium dioxide
with a
rutilization temperature of at least 1000 ~ C, preferably at least 1060 ~ C,
and a sulfate level,
expressed as S03, of at most 1 wt.%, preferably less than 0.8%, for the
preparation of
titanium dioxide based colored pigments.
The following examples are for the purpose of facilitating comprehension of
the
invention without restricting it.
- Determination of the rutilization temperatures of anatase titanium
dioxides.
The samples used in the examples have the following characteristics:
- sample 1: GS powder marketed by the Rhone Poulenc Company. This titanium
dioxide has a BET specific surface of 300 m2/g and a sulfate level, expressed
as S03, of
less than 0.8 wt.%; the powder is in the form of an agglomerate of particles,
with the
average size of the agglomerates close to 1.5 p,m.
- sample 2: comparative powder having a BET specific surface of over 250 m2/g
and a sulfate level, expressed as 503, of 5 wt.%; it is in the form of
agglomerates of
particles, with the average size of the agglomerates close to 1.5 Vim.
The rutilization temperatures of these samples are measured as follows.
First, the reference samples powders are studied by high temperature x-ray
di~action. As a reference for the location of the bands corresponding to the
anatase and
rutile phases, 100% anatase and 100% rutile powders are used. Each reference
powder to
be tested is placed on a flat platinum substrate situated in a closed chamber.
The
temperature of the chamber is progressively increased at a heating speed of 5
~ C/min.
Dif&actograms are drawn at the temperatures of 650, 700, 750, 800, 850, 900,
950, 1000,
1050, 1100, 1150, 1200 and 1250~C, respectively, under the following
conditions:
- acquisition time: 10 s
- angular range 10 ~ to 60 ~ in steps of 0.032 ~ .
The bands corresponding to the rutile and anatase phases are located.

CA 02268076 1999-03-30
::.
7
The same measurements are made on samples 1 and 2. The dif&actograms
obtained enable the evaluation of the percentage of the rutile and anatase
phases by
comparing the surface area of the most intense bands of the two phases with
those marked
on the dif&actograms drawn from the reference samples.
The results are then visualized in the form of curves representing the
variation in
the percentage of the rutile or anatase phase as a function of temperature.
These curves,
proposed in figures l and 2, enable an easy graphic determination of the
rutilization
temperature.
Figure 1 corresponds to sample 1, which shows a rutilization temperature of
1080~C.
Figure 2 corresponds to sample 2, which shows a rutilization temperature of
850~C.
Only the powder from sample 1 may be used in the process according to the
invention since its rutilization temperature is greater than 1000 ~ C.
EXAMPLE 2 - Preparation of the anatase titanium dioxide based colored pigments
with a rutilization temperature of 1080~C.
The anatase titanium dioxide powder of sample 1 (cf. example 1 ) is mixed with
chromiurrl oxide (CR203) and antimony oxide (SbZOs). This mixture is formed
into
pellets.
Then these pellets are calcinated for 12 hrs. at 920 ~ C in an oxygen
atmosphere.
Next, the pellets are ground prior to calcinating them again, first for 12
hrs. at 980~C in
an oxygen atmosphere, then for 4 hrs. at 970~C in air. The resulting powder is
ground.
Two samples of orange-colored pigment are prepared,in this manner:
~ sample 3: this has as a total formula (Tio.9Cro.osSbo.os)02
~ sample 4: this has as a total formula (Tio.~Cro,oosSbo.oos)Ox~
The chemical formula of the final compound is adjusted using the respective
quantities of chromium oxide, antimony oxide and titanium dioxide.
The two pigments obtained have been tested from the point of view of color
saturation.

CA 02268076 1999-03-30
::~:;~:v.' ~r~.a
~.
The coloration is quantified here by the chromatic coordinates L*, a* and b*
of
the 1976 CIE system (L*, a*, b*) as defined by the International Commission on
Illumination and listed in the Compendium of French Standards (Recueil des
Normes
Fran~aises (AFNOR)), colorimetric color no. X08-12 (1983). They are determined
using
a DATACOLOR colorimeter marketed by the SCIENTIFIC PACIFIC Company.
L* gives a measurement of reflectance and gives information on the clarity of
the
color.
a* and b* express the colored tendencies:
a value of a* positive indicates red,
a value of a* negative indicates green,
a value of b* positive indicates yellow, and
a value of b* negative indicates blue.
Thus, schematically, L* represents the variation from white to black
(clarity), a*
the variation from green to red and b* the variation from blue to yellow.
The measurements taken from samples 3 and 4 yielded the results reported in
Table 1 below:
TABLE 1
Pi ent L* a* b*
Sam le 3 67.5 24 59
Sam le 4 84 6 3 8
EXAMPLE 3 (comparative) - Preparation of anatase titanium dioxide based
colored
pigments with a rutilization temperature of 850~C.
Two colored pigments (samples 5 and 6) corresponding respectively to total
formulas (Tio.9Cra.oSSbo.os)OZ ~d (Tio.~,Cro.~SSbo.oos)Oz ~'e prepared
starting from the
anatase titanium dioxide of sample 2 as described in example 1 in accordance
with the
operating mode of example 2.
The measured chromatic data. are reported in table 2 below:
TABLE 2
Pi ent L* a* b*
Sam le 5 66 20 57
Sample 6 -- J g5.g-_I _. 3-2 28.2

CA 02268076 1999-03-30
l-,
:'?
9
It is then noted, by comparing the pigments with the same chemical formula
(samples 3 and 5, on the one hand, and samples 4 and 6, on the other) that the
pigments
according to the invention have higher values for a* and b* and thus, overall,
a more
intense orange-color.
EXAMPLE 4 - Preparation of anatase titanium dioxide based colored pigments
with
a rutilization temperature of 1080~C.
The anatase titanium dioxide used is in sol form. It is marketed by the Rhone
Poulenc Company under reference SS-300. The titanium dioxide in question is
characterized by a BET specific surface of 300 mz/g and a sulfate level,
expressed as S03,
of less than 0.8 wt.% and a rutilization temperature of l 080 ~ C. The dry
extract of the
SS-300 sol is 20 wt.%.
The titanium dioxide colored pigments are prepared by (i) mixing the SS-300
sol
with chromium nitrate and antimony nitrate, (ii) atomization of the resulting
aqueous
mixture, and (iii) calcination/grinding as in example 2.
Two orange-colored samples are thus prepared:
- sample 7 has as a total formula: (Tio.9Cro_osSbo.os)02
- sample 8 has as a total formula: (Tio.99Cro.oosSbo.oos)02~
The chemical formula of the pigments is adjusted using the respective
quantities
of antimony nitrate, chromium nitrate and SS-300 sol.
Samples 7 and 8 were analyzed from the point of view of color saturation. The
results obtained are reported in Table 3. ,
TABLE 3
Pi ent L* a* b*
Sam le 7 68 24 61.5
Sam le 8 85 8 41.2
A comparison of the values for a* and b* in the case of samples 3 and 7, on
the
one hand, and 4 and 8, on the other, reveals a more intense coloration of the
pigments of
samples 7 and 8.

CA 02268076 1999-03-30
.-
'~,y '=~i=''
Thus, it is verified that pigments prepared from an anatase titanium dioxide
sol
according to the invention result in an intensification of shades.

Representative Drawing

Sorry, the representative drawing for patent document number 2268076 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
Time Limit for Reversal Expired 2002-09-30
Application Not Reinstated by Deadline 2002-09-30
Deemed Abandoned - Failure to Respond to Maintenance Fee Notice 2001-10-01
Letter Sent 2000-11-06
Request for Examination Received 2000-09-27
Request for Examination Requirements Determined Compliant 2000-09-27
All Requirements for Examination Determined Compliant 2000-09-27
Letter Sent 1999-08-24
Inactive: Single transfer 1999-07-23
Inactive: Cover page published 1999-05-31
Inactive: Courtesy letter - Evidence 1999-05-12
Inactive: First IPC assigned 1999-05-10
Inactive: Notice - National entry - No RFE 1999-05-10
Inactive: IPC assigned 1999-05-10
Application Received - PCT 1999-05-07
Application Published (Open to Public Inspection) 1998-04-16

Abandonment History

Abandonment Date Reason Reinstatement Date
2001-10-01

Maintenance Fee

The last payment was received on 2000-09-07

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.

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
Basic national fee - standard 1999-03-30
Registration of a document 1999-07-23
MF (application, 2nd anniv.) - standard 02 1999-09-29 1999-09-22
MF (application, 3rd anniv.) - standard 03 2000-09-29 2000-09-07
Request for examination - standard 2000-09-27
Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
MILLENNIUM INORGANIC CHEMICALS S.A.
Past Owners on Record
DENIS HUGUENIN
THIERRY CHOPIN
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) 
Description 1999-03-30 10 488
Abstract 1999-03-30 1 56
Claims 1999-03-30 2 74
Drawings 1999-03-30 1 14
Cover Page 1999-05-28 1 31
Reminder of maintenance fee due 1999-06-01 1 112
Notice of National Entry 1999-05-10 1 194
Courtesy - Certificate of registration (related document(s)) 1999-08-24 1 140
Acknowledgement of Request for Examination 2000-11-06 1 180
Courtesy - Abandonment Letter (Maintenance Fee) 2001-10-29 1 183
PCT 1999-03-30 30 1,261
Correspondence 1999-04-12 1 32