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Patent 2576355 Summary

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(12) Patent: (11) CA 2576355
(54) English Title: TREATMENT OF WASTE USING THREE TEMPERATURE STAGES WITHIN ONE CHAMBER
(54) French Title: PROCEDE DE TRAITEMENT THERMIQUE DES DECHETS PHARMACEUTIQUES
Status: Deemed expired
Bibliographic Data
(51) International Patent Classification (IPC):
  • B09B 3/00 (2006.01)
  • A61L 11/00 (2006.01)
  • C02F 11/10 (2006.01)
  • F23G 7/06 (2006.01)
  • F26B 3/00 (2006.01)
(72) Inventors :
  • CLARKE, STEPHEN (Canada)
(73) Owners :
  • PHASE SEPARATION SOLUTIONS INC. (Canada)
(71) Applicants :
  • PHASE SEPARATION SOLUTIONS INC. (Canada)
(74) Agent: RIDOUT & MAYBEE LLP
(74) Associate agent:
(45) Issued: 2009-07-21
(22) Filed Date: 2007-01-25
(41) Open to Public Inspection: 2008-07-25
Examination requested: 2007-01-25
Availability of licence: N/A
(25) Language of filing: English

Patent Cooperation Treaty (PCT): No

(30) Application Priority Data: None

Abstracts

English Abstract

There is provided a process for the thermal treatment of waste materials, particularly pharmaceutical waste materials. The process comprises placing the waste material into a chamber and increasing the temperature inside the chamber in three stages. At a first stage, water in the material is desorbed as water vapor. At a second stage, organic ingredients in the material are desorbed and decomposed producing condensable organic vapor and non-condensable synthesis gas. And at a third stage, polymer-based components of the material are depolymerized and decomposed producing condensable hydrocarbon vapor. The non-condensable synthesis gas produced can be used as heating source for the process.


French Abstract

Procédé de traitement thermique des déchets, notamment des déchets pharmaceutiques. Le procédé comprend le placement des déchets dans une chambre et l'accroissement en trois étapes de la température à l'intérieur de la chambre. € la première étape, l'eau dans les déchets est désorbée en vapeur d'eau. € la deuxième étape, les ingrédients biologiques dans les déchets sont désorbés et décomposés, produisant de la vapeur organique condensable et des gaz de synthèse non condensables. € la troisième étape, les composants à base de polymères des déchets sont dépolymérisés et décomposés, produisant de la vapeur d'hydrocarbure condensable. Le gaz de synthèse non condensable produit peut servir à produire de la chaleur pour le procédé.

Claims

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



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WHAT IS CLAIMED IS:

1. A process for the thermal treatment of waste material in a chamber,
the process comprising the steps of:
a) heating the chamber at a first temperature to cause water in the
material to desorb as water vapor;
b) heating the chamber at a second temperature higher than the
first temperature to cause organic ingredients in the material to desorb and
decompose producing condensable organic vapor and non-condensable
synthesis gas; and
C) heating the chamber to a third temperature higher than the
second temperature to cause polymer-based components of the material to
depolymerize and decompose producing condensable hydrocarbon vapor,
wherein the material in the chamber is subjected to continuous agitation.
2. A process for the thermal treatment of waste material in a chamber,
the process comprising the steps of:
a) heating the chamber at a first temperature to cause water in the
material to desorb as water vapor;
b) heating the chamber at a second temperature higher than the
first temperature to cause organic ingredients in the material to desorb and
decompose producing condensable organic vapor and non-condensable
synthesis gas; and
c) heating the chamber to a third temperature higher than the
second temperature to cause polymer-based components of the material to
depolymerize and decompose producing condensable hydrocarbon vapor,
wherein the atmosphere inside the chamber is an inert atmosphere.

3. A process for the thermal treatment of waste material in a chamber,
the process comprising the steps of:
a) heating the chamber at a first temperature to cause water in the
material to desorb as water vapor;
b) heating the chamber at a second temperature higher than the


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first temperature to cause organic ingredients in the material to desorb and
decompose producing condensable organic vapor and non-condensable
synthesis gas; and
c) heating the chamber to a third temperature higher than the
second temperature to cause polymer-based components of the material to
depolymerize and decompose producing condensable hydrocarbon vapor,
wherein the material in the chamber is subjected to continuous agitation,
and the atmosphere inside the chamber is an inert atmosphere.

4. A process as defined in any one of claims 1 to 3, wherein the water
vapor, the condensable organic vapor and the condensable hydrocarbon
vapor are continuously recovered and condensed as an oil-water mixture.
5. A process as defined in any one of claims 1 to 3, wherein the non-
condensable synthesis gas is continuously recovered as fuel for combustion
or for heating.

6. A process as defined in any one of claims 1 to 3, wherein the first
temperature is about 100°C, the second temperature is about 250 to
350°C
and the third temperature is about 350 to 500°C.

7. A process as defined in any one of claims 1 to 3, wherein the waste
material is derived from industrial wastes selected from pharmaceutical,
petrochemical, packaging, plastics manufacturing, mining, petroleum
refining, paint and ink manufacturing, sludges and mixtures thereof; or the
waste material is a cellulose material, a polyolefin-based resin, used tires,
contaminated soils or mixtures thereof.

8. A process as defined in any one of claims 1 to 3, wherein the waste
material is a pharmaceutical waste material.

9. A process as defined in any one of claims 1 to 3, wherein the waste
material is subjected to a size reduction step prior to being placed into the
chamber.


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10. A process as defined in claim 5, wherein the non-condensable synthesis
gas is used as heat source for the process.

11. A process as defined in claim 4 further comprising separating oil and
water from the oil-water mixture.

12. A process as defined in claim 9, wherein the size reduction step com-
prises shredding the waste material to obtain particles having a size of less
than about 30 mm.

13. A process as defined in any one of claims 1 to 3, wherein heat is
transmitted to the chamber through its external surface, the heat stemming
from a heating source selected from hot oil, electrical resistance heating,
induction heating and flue of the non-condensable synthesis gas.

14. A process as defined in any one of claims 1 to 3, wherein the pressure
inside the chamber is negative.

15. A process as defined in any one of claims 1 to 3, wherein the
atmosphere inside the chamber is substantially free of oxygen.
16. A process as defined in claims 2 or 3, wherein an inert gas is
introduced into the chamber, the inert gas being nitrogen or argon.

17. A process as defined in any one of claims 1 to 3 further comprising
recovering treated waste material from the chamber, the treated waste
material having a volume which is about 90% reduced.

18. A process for the thermal treatment of waste material in a chamber,
the process comprising the steps of:
a) heating the chamber at a first temperature to cause water in the
material to desorb as water vapor;
b) heating the chamber at a second temperature higher than the




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first temperature to cause organic ingredients in the material to desorb and
decompose producing condensable organic vapor and non-condensable
synthesis gas;
c) heating the chamber to a third temperature higher than the
second temperature to cause polymer-based components of the material to
depolymerize and decompose producing condensable hydrocarbon vapor;
d) continuously recovering oil, water, hydrocarbon vapor and non-
condensable synthesis gas, the non-condensable synthesis gas being used
as heat source for the process; and
e) recovering treated waste material from the chamber, the treated
waste material having a volume which is about 90% reduced,
wherein the material in the chamber is subjected to continuous agitation.

19. A process for the thermal treatment of waste material in a chamber,
the process comprising the steps of:
a) heating the chamber at a first temperature to cause water in the
material to desorb as water vapor;
b) heating the chamber at a second temperature higher than the
first temperature to cause organic ingredients in the material to desorb and
decompose producing condensable organic vapor and non-condensable
synthesis gas;
c) heating the chamber to a third temperature higher than the
second temperature to cause polymer-based components of the material to
depolymerize and decompose producing condensable hydrocarbon vapor;
d) continuously recovering oil, water, hydrocarbon vapor and non-
condensable synthesis gas, the non-condensable synthesis gas being used
as heat source for the process; and
e) recovering treated waste material from the chamber, the treated
waste material having a volume which is about 90% reduced,
wherein the atmosphere inside the chamber is an inert atmosphere.


20. A process for the thermal treatment of waste material in a chamber,
the process comprising the steps of:
a) heating the chamber at a first temperature to cause water in the




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material to desorb as water vapor;
b) heating the chamber at a second temperature higher than the
first temperature to cause organic ingredients in the material to desorb and
decompose producing condensable organic vapor and non-condensable
synthesis gas;
c) heating the chamber to a third temperature higher than the
second temperature to cause polymer-based components of the material to
depolymerize and decompose producing condensable hydrocarbon vapor;
d) continuously recovering oil, water, hydrocarbon vapor and non-
condensable synthesis gas, the non-condensable synthesis gas being used
as heat source for the process; and
e) recovering treated waste material from the chamber, the treated
waste material having a volume which is about 90% reduced,
wherein the material in the chamber is subjected to continuous agitation,
and the atmosphere inside the chamber is an inert atmosphere.


21. A process as defined in any one of claims 18 to 20, wherein the first
temperature is about 100°C, the second temperature is about 250 to
350°C
and the third temperature is about 350 to 500°C.


22. A process as defined any one of claims 18 to 20, wherein the waste
material is a pharmaceutical waste material.


23. A process as defined any one of claims 18 to 20, wherein the waste
material is subjected to a size reduction step prior to being placed into the
chamber.


24. A process as defined any one of claims 18 to 20, wherein heat is
transmitted to the chamber through its external surface, the heat stemming
from a heating source selected from hot oil, electrical resistance heating,
induction heating and flue of the non-condensable synthesis gas.


25. A process as defined in claim 19 or 20, wherein an inert gas is
introduced into the chamber, the inert gas being nitrogen or argon.





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26. A process as defined in any one of claims 18 to 20, wherein the
pressure inside the chamber is negative.

Description

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



CA 02576355 2008-07-29

TITLE OF THE INVENTION

TREATMENT OF WASTE USING THREE TEMPERATURE STAGES
WITHIN ONE CHAMBER

FIELD OF THE INVENTION

The invention relates generally to processes for the thermal treatment
of waste materials. In particular, the invention relates to a process for the
thermal treatment of pharmaceutical waste materials, and subsequent
recovery of oil.

BACKGROUND OF THE INVENTION

Disposal of waste materials, in particular hazardous and non-
hazardous pharmaceutical and personal consumer product waste, has
generally been completed primarily through shredding and landfilling. While
shredding removes potential product liability issues such as black market re-
selling of off-spec and expired products as well as unwanted public visibility
of corporate identifiers, the desire to reduce the volume of waste to be
landfilled has led to the development of alternative processes such as
recycling, composting and incineration. These processes have some
benefits but also present significant disadvantages. For example, not all
components of the waste stream present sufficient economic value to justify
a recycling program. Also, not all components of the waste stream are
suitable for compost production. And incineration is widely known as
requiring high levels of energy and sophisticated equipment as well as
producing airborne emissions; moreover incineration does not allow for the
recovery of hydrocarbons. On the other hand, it is desirable to recover at
least some valuable materials from the waste in order to reduce the
environmental pollutants that may result from their decomposition.
Numerous waste materials comprise medicinal ingredients that are
classified as regulated compounds, and require total destruction. Various
processes allowing for the destruction of these compounds, including


CA 02576355 2007-01-26

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thermal treatment, are known in the art. For example, US 2005/0218037
discloses a process for thermal treatment of multiphase residues. The
process uses a three-stage temperature gradient, wherein the temperature
increases from about 80 to 250 C. Each stage is carried out within a
separate zone of the reactor, and the material to be treated is circulated
from one zone to the other. The process takes place under inert
atmosphere, and yields oil, water, hydrocarbons as well as solid residue. US
6,840,712 discloses a similar process with the temperature increasing from
about 316 to 649 C.

US 4,013,516 and Canadian patents 2,543,320; 2,515,431;
2,313,801; 2,251,004; and 2,423,714 also disclose similar thermal
treatment processes, at various temperature ranges.

There remains a need for simple, environmentally friendly and cost
efficient thermal treatment processes of waste materials.

SUMMARY OF THE INVENTION

The inventors have developed a process that combines desorption,
depolymerization and pyrolysis for the treatment of waste materials,
particularly pharmaceutical waste materials. The material to be treated is
placed in a reaction chamber and subjected to a three-stage gradient
temperature, without any need to circulate the material. The process
ensures residence time at such temperatures as to thermally destroy the
medicinal ingredients. The process also allows for a continuous recovery of
oil, water as well as non-condensable synthesis gas that can be used as
heating source for the process. The process yields a solid residue of
significantly reduced size that is suitable for safe landfilling.

The invention thus provides according to an aspect, for a process for
the thermal treatment of waste material in a chamber. The process
comprises the steps of: a) heating the chamber at a first temperature to
cause water in the material to desorb as water vapor; b) heating the
chamber at a second temperature higher than the first temperature to cause


CA 02576355 2007-01-26

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organic ingredients in the material to desorb and decompose producing
condensable organic vapor and non-condensable synthesis gas; and c)
heating the chamber to a third temperature higher than the second
temperature to cause polymer-based components of the material to
depolymerize and decompose producing condensable hydrocarbon vapor.
The water vapor, the condensable organic vapor and the condensable
hydrocarbon vapor produced in the process can be continuously recovered
and condensed as an oil-water mixture; and the non-condensable synthesis
gas can be continuously recovered as fuel for combustion or for heating.

In a preferred embodiment of the process, the first temperature can
be about 100 C, the second temperature can be about 250 to 350 C and
the third temperature can be about 350 to 500 C.

The process according to the invention can be carried out on various
types of waste materials including but not limited to waste material derived
from industrial wastes such as pharmaceutical, petrochemical, packaging,
plastics manufacturing, mining, petroleum refining, paint and ink manu-
facturing, sludges as well as mixtures thereof. The waste material can also
be a cellulose material, a polyolefin-based resin, used tires, contaminated
soils or mixtures thereof.

In a preferred embodiment of the invention, the waste material is a
pharmaceutical waste material.

The waste materiai may be subjected to a size reduction step prior to
being placed into the chamber. The size reduction step may comprise
shredding the waste material to obtain particles having a size of less than
about 30 mm.

In a preferred embodiment, the non-condensable synthesis gas is
used as heat source for the process. Also, the process can further comprise
a step of separating oil and water from the oil-water mixture.

During the process, heat can be transmitted to the chamber through
its external surface. Optionally, the heat may stem from a heating source


CA 02576355 2007-01-26

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which can be hot oil, electrical resistance heating, induction heating or a
flue
of the non-condensable synthesis gas. The material in the chamber may be
subjected to continuous agitation. The pressure inside the chamber may be
negative, and the atmosphere substantially free of oxygen or inert.
Optionally, an inert gas such as nitrogen or argon can be introduced into the
chamber.

The volume of the treated waste material recovered after the process
may be about 90% reduced.

According to another aspect, the invention provides for a process for
the thermal treatment of waste material in a chamber, the process
comprising the steps of: a) heating the chamber at a first temperature to
cause water in the material to desorb as water vapor; b) heating the
chamber at a second temperature higher than the first temperature to cause
organic ingredients in the material to desorb and decompose producing
condensable organic vapor and non-condensable synthesis gas; c) heating
the chamber to a third temperature higher than the second temperature to
cause polymer-based components of the material to depolymerize and
decompose producing condensable hydrocarbon vapor; d) continuously
recovering oil, water, hydrocarbon vapor and non-condensable synthesis
gas, the non-condensabie synthesis gas being used as heat source for the
process; and e) recovering treated waste material from the chamber, the
treated waste material having a volume which is about 90% reduced.

In a preferred embodiment of this process, the waste materiai is a
pharmaceutical waste material.

These and other aspects of the invention wiil be more clearly seen
from the detailed description of a preferred embodiment outlined below.
DESCRIPTION OF THE DRAWING

Figure 1 is a thermal process flow diagram which illustrates the
process according to the invention.



CA 02576355 2007-01-26

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While the invention will be described in conjuncture with the
illustrated embodiment, it will be understood that it is not intended to limit
the invention to such embodiment. On the contrary, it is intended to cover
all alternatives, modifications and equivalents as may be included within the
spirit and scope of the invention as defined by the appended claims.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS OF THE
INVENTION

As used herein and in the claims, the following terms have the
meaning and definition set out below.

The term "pyrolysis" is meant to encompass processes wherein the
atmosphere in the pyrolysis chamber may contain a small amount of air
(oxygen), but the amount is so small that there is no visible combustion.
Although the term "pyrolysis" is generally defined as the "transformation of
a compound into one or more substances by heat alone, i.e., without
oxidation" (Hawley's Condensed Chemical Dictionary, 13 th Ed. (1997).), it is
envisaged that at least a small amount of oxygen may be present into the
chamber during the process according to the invention. Indeed, some air
may enter the chamber during the loading of the waste. Also some air may
be entrained within the waste. Moreover, as the pressure within the
chamber may be slightly negative, a small amount of air may be drawn into
the furnace through deficient seals for example.

The term "waste material" is meant to refer to any suitable product
that can be subjected to the process according to the invention, including
but not limited to pharmaceutical waste materials. Other streams for which
the process according to the invention is also suitable include but are not
limited to petrochemical, sludges, packaging, plastics manufacturing,
mining, petroleum refining, paint and ink manufacturing as well as mixtures
thereof. The waste material can also be a cellulose-based material,
polyolefin-based resin, used tires or other industrial rubbers, contaminated
soils or mixtures thereof.


CA 02576355 2007-01-26

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The term "non-condensable gas" is meant to refer to a gas which is
not readily condensed, and includes gases such as methane, propane or
butane but also hydrogen, carbon dioxide and carbon monoxide.

The term "depolymerization" is meant to refer to the process of
converting a long chain hydrocarbon-based polymer into a shorter chain
hydrocarbon through a sequence of reactions at certain temperatures.

An embodiment of the process according to the invention will be
described with reference to the accompanying process flow diagram. The
process is carried out in a standard apparatus known in the art.

The waste material to be treated is fed to the reactor hopper. A
series of two dual flapper valves or rotary valves are provided at the base of
the hopper, each valve feeding the reaction chamber where the thermal
process including desorption, depolymerization and pyrolysis, takes place.
The use of dual flapper valves or rotary valves limits the ingress of oxygen
into the chamber. The waste material is introduced into the reaction
chamber at a specific rate which is determined by the valve rate.

In order to facilitate handing and also to have a consistent feedstock,
the waste material is shredded prior to being fed to the reactor hopper.
During this stage there is some degree of decomposition of the medicinal
ingredients through physical breakdown from the shredding action.
Preferably, shreds having a dimension of less than about 30 mm are
formed. Shredding can be carried out on-site or at another location.

The waste material is placed into an indirectly heated thermal
reaction chamber. The reaction chamber is heated externally with hot oil,
electrical resistance heating, induction heating, or flue gas from the
combustion of fuel. The temperature inside the extraction chamber is
controlled by a simple thermal control loop. The pressure in the reaction
chamber can be either positive or negative. Preferably, the pressure inside
the reaction chamber is negative. An inert gas such as nitrogen or argon
can be injected into the chamber such that the process takes place in an
inert atmosphere.


CA 02576355 2007-01-26

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The waste material enters the reaction chamber where it is conveyed
along the length of a steel reaction tube associated with the reaction
chamber, by sloping the said tube. A rotating tube or an auger located
inside the reaction chamber continually agitates the material. Heat is
transmitted to the waste material inside the reaction chamber via
conductive transfer of energy.

Turning to the process flow diagram, at a first stage where the
temperature inside the reactor chamber is maintained at about 100 C,
water in the waste material is desorbed as water vapor, which can be
removed and condensed.

At a second stage, the temperature is increased to about 250 to
350 C, any remaining water from the waste material is desorbed. Also,
active organic ingredients are desorbed then decomposed yielding
condensable organic vapor and non-condensable synthesis gas. At this
stage the condensable organic vapor which may also include some water
vapor, is removed and condensed. And the non-condensable synthesis gas
is also removed.

A further stepped increase in temperature from 350 C to about 500 C
in the reaction chamber beyond desorption, volatilization and decomposition
temperatures results in depolymerization of plastic resins and polymers.
This depolymerization results in the release of condensable hydrocarbons
from their solid state allowing for their recovery and reuse. At this stage,
any organic ingredients that were not decomposed in the second stage, are
decomposed producing hydrocarbon vapor that can be removed through the
same means as the organic vapor. At these temperatures the medicinal
ingredients resident in the pharmaceutical waste product is thermally
decomposed. This decomposition is confirmed via the review of boiling
points and decomposition temperatures of medicinal compounds. Several
common examples are: acetylsalicylic acid (140 C), celebrex (150 C),
acetaminophen (170 C), pseudoephdrine hydrochloride (186 C), minoxidil
(78 C) and metoropol (120 C).


CA 02576355 2007-01-26
- ~ -

Indeed, water vapor, organic vapor and hydrocarbon vapors can be
removed together and condensed as a mixture of oil-water. And the
mixture of oil and water can further be subjected to a separation step to
yield oil and water. The non-condensable synthesis gas can be used as
heating source for the process.

The vapors and gases in the reaction chamber are removed either
under pressure or by vacuum. The vapors and gases are preferably
removed under vacuum. The vapors can be condensed into a liquid using a
heat exchanger, quenched with water or with any suitable type of oil
fraction similar to diesel. In the case where a recirculating water quench
system is used, the condensed oil and water from the process can be
separated in an oil water separator and the water fraction is cooled with a
heat exchanger and recycled to the quench. In the case where a
recirculating oil quench is used, the quenched oil and water can be
separated in an oil water separator and the oil fraction is cooled with a heat
exchanger and recycled to the quench. In any of these cases, excess oil
and water is continuously removed from the process approximately
proportional to the mixed waste feed content.

During the process a volume of condensable vapors and non-
condensable gases are generated. The condensable hydrocarbons vapors
are recovered in a liquid state as described above. The non-condensable
gases include methane, propane, butane as well as hydrogen, carbon
dioxide and carbon monoxide. These gases can be filtered for further
removal of particulate and fine mist and final polishing using activated
carbon. The non-condensable gases are commonly referred to as synthesis
gas and can be combusted to generate energy for the process or to
generate steam for power generation.

The hydrocarbon extracted is similar in terms of its composition to
No. 2 Fuel Oil or Diesel and is suitable for reuse or further fractional
distillation. A mass balance of the process generates the following outputs
based on the input feed characteristics described above.


CA 02576355 2007-01-26

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A certain fraction of the material remains from the process as an inert
carbonaceous mass. This solid residue is removed from the reaction
chamber using a rotary paddle airlock into a water based cooling system
prior to being discharged.

Table 1 outlines an example of composition of a sample that can be
treated according to the process of the invention.

Table 1

Summary Mixed By wt
Pharmaceutical
Plastic Bottles 35%
Medicinal ingredients 10%
Paper (cellulose) 20%
Inert Solids & Foil 25%
Other Liquids 10%
100%
Table 2 outlines an example of relative amounts of the products
obtained after treatment by the process of the invention.
Table 2

Total
Byproducts
Oil 35%
Gas 16%
Carbon/Inert 32%
Solids
Water 17%
100%
Thus it is apparent that there has been provided in accordance with
the invention a process for the thermal treatment of waste materials, in
particular pharmaceutical waste materials. The process combines
desorption, depolymezation and pyrolysis; and is simple, environmentally


CA 02576355 2007-01-26

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friendly and cost efficient. While the invention has been described in
conjunction with the illustrated embodiment, it is evident that many
alternatives, modifications and variations will be apparent to those skilled
in
the art in light of the foregoing description. Accordingly, it is intended to
embrace all such alternatives, modifications and variations as fall within the
spirit and broad scope of the invention.

Representative Drawing
A single figure which represents the drawing illustrating the invention.
Administrative Status

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 , Administrative Status , Maintenance Fee  and Payment History  should be consulted.

Administrative Status

Title Date
Forecasted Issue Date 2009-07-21
(22) Filed 2007-01-25
Examination Requested 2007-01-25
(41) Open to Public Inspection 2008-07-25
(45) Issued 2009-07-21
Deemed Expired 2019-01-25

Abandonment History

There is no abandonment history.

Payment History

Fee Type Anniversary Year Due Date Amount Paid Paid Date
Request for Examination $400.00 2007-01-25
Registration of a document - section 124 $100.00 2007-01-25
Application Fee $200.00 2007-01-25
Maintenance Fee - Application - New Act 2 2009-01-26 $50.00 2009-01-21
Final Fee $150.00 2009-01-29
Maintenance Fee - Patent - New Act 3 2010-01-25 $50.00 2009-10-29
Maintenance Fee - Patent - New Act 4 2011-01-25 $50.00 2010-12-01
Maintenance Fee - Patent - New Act 5 2012-01-25 $100.00 2011-12-19
Registration of a document - section 124 $100.00 2012-11-15
Maintenance Fee - Patent - New Act 6 2013-01-25 $100.00 2012-12-17
Maintenance Fee - Patent - New Act 7 2014-01-27 $100.00 2013-08-16
Registration of a document - section 124 $100.00 2013-10-07
Registration of a document - section 124 $100.00 2013-10-07
Maintenance Fee - Patent - New Act 8 2015-01-26 $100.00 2015-01-19
Maintenance Fee - Patent - New Act 9 2016-01-25 $100.00 2016-01-19
Maintenance Fee - Patent - New Act 10 2017-01-25 $125.00 2016-10-04
Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
PHASE SEPARATION SOLUTIONS INC.
Past Owners on Record
CLARKE, STEPHEN
Past Owners that do not appear in the "Owners on Record" listing will appear in other documentation within the application.
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Document
Description 
Date
(yyyy-mm-dd) 
Number of pages   Size of Image (KB) 
Description 2008-07-29 10 397
Drawings 2008-07-29 1 15
Claims 2008-07-29 6 208
Abstract 2007-01-26 1 19
Description 2007-01-26 10 396
Claims 2007-01-26 4 113
Cover Page 2008-07-18 1 32
Representative Drawing 2008-11-06 1 12
Cover Page 2009-06-25 2 47
Drawings 2007-01-26 1 23
Prosecution-Amendment 2008-07-29 12 372
Correspondence 2009-01-29 2 44
Assignment 2007-01-26 3 106
Prosecution-Amendment 2008-05-23 2 86
Fees 2009-01-21 2 74
Correspondence 2009-01-21 2 74
Correspondence 2009-01-13 1 28
Fees 2009-10-29 1 35
Fees 2010-12-01 1 36
Assignment 2012-11-15 39 1,886
Correspondence 2013-07-05 1 23
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