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Sommaire du brevet 2165633 

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Disponibilité de l'Abrégé et des Revendications

L'apparition de différences dans le texte et l'image des Revendications et de l'Abrégé dépend du moment auquel le document est publié. Les textes des Revendications et de l'Abrégé sont affichés :

  • lorsque la demande peut être examinée par le public;
  • lorsque le brevet est émis (délivrance).
(12) Brevet: (11) CA 2165633
(54) Titre français: METHODE D'ALIMENTATION EN REACTIF ET EN AIR D'OXYDATION
(54) Titre anglais: METHOD OF REAGENT AND OXIDATION AIR DELIVERY
Statut: Périmé et au-delà du délai pour l’annulation
Données bibliographiques
(51) Classification internationale des brevets (CIB):
  • B01D 53/80 (2006.01)
  • B01D 53/50 (2006.01)
(72) Inventeurs :
  • ROGERS, KEVIN JOHN (Etats-Unis d'Amérique)
  • JOHNSON, DENNIS WAYNE (Etats-Unis d'Amérique)
(73) Titulaires :
  • THE BABCOCK & WILCOX COMPANY
(71) Demandeurs :
  • THE BABCOCK & WILCOX COMPANY (Etats-Unis d'Amérique)
(74) Agent: SMART & BIGGAR LP
(74) Co-agent:
(45) Délivré: 1999-05-18
(22) Date de dépôt: 1995-12-18
(41) Mise à la disponibilité du public: 1996-06-20
Requête d'examen: 1995-12-18
Licence disponible: S.O.
Cédé au domaine public: S.O.
(25) Langue des documents déposés: Anglais

Traité de coopération en matière de brevets (PCT): Non

(30) Données de priorité de la demande:
Numéro de la demande Pays / territoire Date
08/359,147 (Etats-Unis d'Amérique) 1994-12-19

Abrégés

Abrégé français

Une méthode de désulfuration de gaz de carneau par oxydation forcée utilise un flux d'air à système d'air d'oxydation non seulement pour alimenter un réservoir d'absorbeur en air d'oxydation, mais également pour véhiculer par air comprimé et injecter un réactif anhydre dans le réservoir d'absorbeur, de façon à satisfaire aux critères d'addition de réactif. Si nécessaire, d'autres additifs anhydres peuvent être ajoutés au réactif anhydre, de telle façon que le flux d'air d'oxydation injecte à la fois le réactif anhydre et les additifs anhydres dans le réservoir de l'absorbeur. Avec cette méthode, les additifs anhydres peuvent être ajoutés même si le réactif est introduit par d'autres méthodes connues.


Abrégé anglais


A method of forced oxidation flue gas desulfurization uses an oxidation air system
air stream to not only provide oxidation air into an absorber vessel, but also to pneumatically
convey and inject dry reagent into the absorber vessel to satisfy reagent addition
requirements. If necessary, other dry additives can be added to the dry reagent so that the
oxidation air stream injects both the dry reagent and the dry additives into the absorber
vessel. The dry additives can be added in this method even if the reagent is introduced by
other known methods.

Revendications

Note : Les revendications sont présentées dans la langue officielle dans laquelle elles ont été soumises.


THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A method of forced oxidation flue gas desulfurization, wherein dry reagent and dry
additive are pneumatically supplied to an absorber vessel containing a liquid slurry through
an oxidation air addition system, comprising:
providing a rate controlled feed supply of prepared dry reagent selected from the
group consisting of solid alkali compounds used in flue gas desulfurization processes
including calcium, potassium, aluminum, sodium and ammonium compounds and dry
additive used to promote at least one of the functions selected from the group consisting
of promoting oxidation, enhancing chemical absorption of SO2 from the flue gas provided
to the absorber vessel, providing buffering and promoting crystallization to a pneumatic
conveying pick-up point located within air supply piping used to provide an oxidation air
stream from the oxidation air addition system into the absorber vessel;
controlling a feed rate of the dry reagent to the pneumatic conveying pick-up point
independently of a feed rate of the oxidation air stream into the absorber vessel;
using the oxidation air addition system air stream as the sole means of providing
oxidation air into the absorber vessel, and to pneumatically convey and inject the dry
reagent and dry additive into the absorber vessel to at least partially desulfurize flue gas
provided to the absorber vessel; and
injecting the oxidation air stream, the dry reagent, and the dry additive beneath a
liquid surface level of the liquid slurry within the absorber vessel.
2. The method according to claim 1, wherein the dry reagent injected into the
absorber vessel via the oxidation air addition system is sufficient to completely desulfurize
flue gas provided to the absorber vessel.
3. The method according to claim 1, further including the step of adding the dryadditive to the dry reagent so that the oxidation air stream injects both the dry reagent and

the dry additive into the absorber vessel.
4. The method according to claim 1, further including the step of providing a
minimum feed rate oxidation air stream whenever the feed rate of the dry reagent is
greater than zero, to prevent solids dropout in the air supply piping.
5. The method according to claim 1, further including the step of pneumatically
conveying the dry reagent to the pneumatic conveying pick-up point located within the
air supply piping.
6. The method according to claim 1, further including the step of injecting the dry
reagent and the dry additive into the absorber vessel in the vicinity of a dispersion means
to enhance dispersion of the oxidation air stream, the dry reagent, and the dry additive
within the liquid slurry contained within the absorber vessel.
7. The method according to claim 1, wherein the dry additive is added in catalytic
amounts to promote oxidation within the absorber vessel and is a member selected from
the group consisting of compounds of iron, manganese, and vanadium.
8. The method according to claim 1, wherein the reagent is lime or limestone and the
dry additive is a member selected from the group consisting of alkali compounds of
magnesium, ammonium, potassium, calcium, and sodium.
9. The method according to claim 1, wherein the dry additive is a buffering agent for
the desulfurization occurring within the absorber vessel and is a member selected from the
group consisting of sodium formate, dibasic acid (DBA), sodium citrate, adipic acid,
succinic acid, and solid compounds of formic, acetic, hydroxypropionic, sulfosuccinic,
adipic, phthalic, benzoic, fumaric, hydroxyacetic, succinic, and lactic acid.

11
10. The method according to claim 1, wherein the dry additive is a member selected
from the group consisting of compounds of formate and thiosulfate and elemental sulfur.
11. The method according to claim 1, wherein the dry additive is polysulfonate.
12. A method of forced oxidation flue gas desulfurization, wherein dry additive is
pneumatically supplied through an oxidation air addition system to an absorber vessel
containing a liquid slurry, comprising:
providing into the absorber vessel at least one reagent selected from the group
consisting of solid alkali compounds used in flue gas desulfurization processes including
calcium, potassium, aluminum, sodium and ammonium compounds;
providing a rate controlled feed supply of dry additive used to promote at least one
of the functions selected from the group consisting of promoting oxidation, enhancing
chemical absorption of SO2 from the flue gas provided to the absorber vessel, providing
buffering and promoting crystallization to a pneumatic conveying pick-up point located
within air supply piping used to provide an oxidation air stream from the oxidation air
addition system into the absorber vessel;
controlling a feed rate of the dry additive to the pneumatic conveying pick-up point
independently of a feed rate of the oxidation air stream into the absorber vessel;
using the oxidation air addition system air stream as the sole means of providing
oxidation air oxidation air into the absorber vessel, and to pneumatically convey and inject
the dry additive into the absorber vessel; and
injecting the oxidation air stream, and the dry additive beneath a liquid surface level
of the liquid slurry within the absorber vessel.
13. The method according to claim 12, wherein the dry additive is added in catalytic
amounts to promote oxidation within the absorber vessel and is a member selected from
the group consisting of compounds of iron, manganese, and vanadium.

12
14. The method according to claim 12, wherein the reagent is lime or limestone and
the dry additive is a member selected from the group consisting of alkali compounds of
magnesium, ammonium, potassium, calcium, and sodium.
15. The method according to claim 12, wherein the dry additive is a buffering agent
for the desulfurization occurring within the absorber vessel and is a member selected from
the group consisting of sodium formate, dibasic acid (DBA), sodium citrate, adipic acid,
succinic acid, solid compounds of formic, acetic, hydroxypropionic, sulfosuccinic, adipic,
phthalic, benzoic, fumaric, hydroxyacetic, succinic, and lactic acid.
16. The method according to claim 12, wherein the dry additive is added to inhibit
oxidation to reduce scale growth within the absorber vessel and is a member selected from
the group consisting of compounds of formate and thiosulfate and elemental sulfur.
17. The method according to claim 12, wherein the dry additive is polysulfonate.

Description

Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.


CASE5580 2165633
..
METHOD OF REAGENT AND OXIDATION AIR DELIVERY
FIELD AND BACKGROUND OF THE INVENTION
The present invention relates in general to wet flue gas desulfurization (FGD)
processes and, in particular, to wet lim.os~on~ forced o~i-li7~ flue gas desulfurization
5 ~roc~es (LSFO-FGD) pr~sses and other cn.,-pAIihle procesæs. Wet LSFO-FGD systems
have s~ ox~ tion air and l;...~(o~e slurry streams. Theæ systems, in general, utilize
a wet ~ g circuit by ~ coarse 1;...~ f to prepare a limeston~ solids-liquid slurry
as the fresh reagent supplied to the absorber system. Typically, wet ball mills have been
used for ~is ~u.~ose. The wet CO~ m process has the advaD~age of ~ot~ ially lower
0 hOlY~ l~Ui~ than dry ~ ;. N1;. ~ ploce~xs, and the fact that the end product after
is a slurry also fits in well with the wet LSFO-FGD system design. This slurry is
commonly stored in a holding tank to provide surge c~a~i~y for :~ubse(lu.,.l~ controlled
supply to the absorber vessel based on l~m~n(3,
In wet FGD ~,.~ lls, the sulfur dioxide (SO2) absol~io~ ~locess l~u~s a nearly
lS contimloll~ supply of fresh l~e~ to ~ s~ti~f~-tory oper~tion and SO2 removal

CASE ~80 2 1 6 5 6 3 3
efficiencies. Often it is desirable to incorporate air addition to the wet FGD absorber to
provide in situ forced oxidation of the absorber reaction product.
Providing se~ e o~da~ll air and ;i....o~1...~ slurry streams increases the complexity
and expense of these- wet LSFO~G-l}systerns. -lt is thus apparent that an approach to
S providing these se~ala~ functions in a simple and cost-effective manner would be welcomed
by the industry.
SUMMARY OF THE INVENTION
The filn~m~n~l nature of the present invention is the use of the oxidation air system
air stream to not only provide oxidation air to an absorber vessel, but also to both
l0 pneumatically convey and inject dry reagent into the absorber vessel to satisfy reagent
addition requirements.
Accordingly, one aspect of the present invention is drawn to a method of forced
oxidation flue gas desulrul~lion wherein dry reagent and dry additive are supplied to an
absorber vessel cont~ining a liquid slurry through an oxidation air addition system. The
15 method colllylises the steps of: providing a rate controlled feed supply of ~r~ared dry
reagent and dry additive to a ~.~r.. AIic collv~ying pick-up point located within air supply
piping used to provide an oxidation air stream from the oxidation air addition system into
the absorber vessel; and using the oxidation air addition system air stream to provide
ox~ tion air into the abso~ vessel, and to ~ lly convey and inject the dry reagent
20 and dry addilive into the absoll~r vessel sufficient to partially desulfurize flue gas provided
to the al)so~ vessel.
The dry reagent is a ~ ~L ~1P~d from the group cO.~icli..g of solid alkali
colll~oullds used in flue gas desulruli~lion ~r(xesses inrl~lAing lillles~o~e, e~1cillm,
~o1~ c--.. ", ~1.. ;.. , so linm, and/or ~mmonillm colll~ullds. Other dry additives besides
25 reagent can be added sepz. ~ ly or added to the dry reagent so that the oxi-l~tion air stream
inje ts both the dry reagent and the dry additives into the absoll,cl vessel. These additives
could be added to promote oxi~ti~)n ~,vithin the absorber vessel; to ~ A.~-e cl~ ;r~l
al)sol~liol~ of the SO2 within the al)sollJcr vessel or to provide a desired degree of b~rL~ g
to the ~ lrl.. ;,,.~ion ~locess ~ ih; to inhibit scale growth vithin the al)soll~r vessel; or

CASE5580 - 2165633
to promote or specify the type of or degree of cryst~lli7~tion7 etc., in the desulfuri_ation
process occurring within the absorber vessel.
Acco,dil,~,ly, another aspect of the present invention is drawn to a method of forced
oxidation flue gas desulfurization, wherein.~dry~-r~litive i~ r.~ tir~lly supplied to an
absorber vessel cont~ining a liquid slurry through an oxidation air addition system. The
steps of this method conl~lise: providing a rate controlled feed supply of prepared dry
additive to a pn~nm~tic conveying pick-up point located within air supply piping used to
provide an oxidation air stream from the oxidation air addition system into the absorber
vessel; and using the oxidation air addition system air stream to provide oxidation air into
the abso,l,ci vessel, and to ~ ir~lly convey and inject the dry additive into the absorber
vessel.
The various feat~lrcs of novelty which characteri_e the invention are pointed out with
particularity in the claims annexed to and forming a part of this disclosure. For a better
underst~n-~in~ of the invention, its opela~ing advantages and specific results ~tt~in~A by its
uses, refc,c,lce is made to the ~ ol--p~.-yhlg drawings and descfl~live matter in which a
~ref~.,ed embodiment of the invention is illustrated.
BRIEF DESCRIPIION OF THE DRAWINGS
In the drawings:
Fig. 1 is a s~ P-~ ;c illllstr~tion of a system according to a first emb~im~nt of the
present invention; and
Fig. 2 is a sc-~ s~tion of a system acco~ing to a second embodiment of
the present invention.
DESCRIPTION OF THE PREFFRRFn EMBODIMENT
In the d~s, l~e mlm~o.r~lc ~ ". ~ the same or similar elem~o-nt~ throughout the
two drawings. ~.f~ to Fig. 1 in particular, one aspect of the present invention is
drawn to a system 10 using a m.o.th~1 of forced o~i~3ati~n flue gas ~e~llr~ lion~ wllc~ehl
dry reagent is ~u~pli~d to an absollc~ vessel, s~ lly shovn at 11, through an
o~ tion air ~l-lition system. A p~ly p~ ,d reagent 12 in a dry form is IL~s~lL~d

CASE5580 2165633
to a reagent surge bin 14, either by m~h_nir~l conveyance, or by dilute or dense phase
conveyance, through a supply line 16. The dry reagent 12 is withdrawn from the surge bin
14 at a controlled rate by feeder means 18, such as a volumetric or gravimetric feeder. The
controlled feed rate of dry reagent 12 corresponds to an absorber.-reagent ~m~n(1 required
S by the absorber vessel 11. The feeder means 18 discl~ges to a gravity flow chute 20 which
directs the dry reagent 12 to an airlock 22. The airlock 22 provides the required level of
isolation between the gravity flow chute 20 and an oxidation air stream 24 provided from
oxidation air supply means 25, such as a blower or COlllpl~,SSOi station, at a higher pressure
via o~ tion air line supply piping 26. Oxidation air 24 which leaks across the airlock 22
can be vented through a vent filter 28 and into the atmosphere 30. Dry reagent 12 which
passes through the airlock 22 is introduced to the oxidation air line 26 at a solid pn~nm~tic
conveying pick-up point 32, incorporated within the air line supply piping 26 used to provide
the oxidation air stream 24 into the absorber vessel 11. The oxidation air stream 24
sl~bs~~ ntly provides oxidation air to the absorber vessel 11, and pn~llm~tir~lly conveys and
lS injects the dry reagent 12 to the absol~r vessel 11 through line 34 to partially or completely
satisfy the reagent addition requir~-m~nt~.
The dry reagent 12 is a m.omher selected from the group con~i~ting of solid alkali
col~ds used in flue gas le~llr~ ;on plocesses such as limestone, calcium, pot~inm,
~lnmimlm, sodiurn, and/or ammonium. Dry additives 36 can be added to the dry reagent
20 12 into the surge bin 14 by "~ a.,;~al con~ ~, or by dilute or dense phase collvey~ce~
through dry additive supply line 37, so that the oxidation air stream 24 injects both the dry
reagent 12 and the dry addilivcs 36 into absorber vessel 11. The dry additives 36 could also
be added s~ t~_ly into the o~ i~1al i~ air stream 24 at the same p ~ "~ COll~ illg pick-up
point 32, or at uy~ll~ or dow~ll~ dry addidves y..~ convt;ying pick-up points
38, 39 l~sye~ y. Various dry additives 36 could be added to promote oxidation within
the absoll,c~ vessel 11; to c~ A.~e cl~...i~al absorption of the SO2 within the absoll~. vessel
11 or to provide a desired degree of b..rr~ to the ~les~lr~ ;on process therein; to
inhibit scale growth within the absol1~ vessel 11; or to promote or specify the type of or
degree of cryst-lli7-tion, etc., in the ~ lr,.. ;,~ ,. process o~ , within the absorber

CASE 5580 2 ~ 6 5 6 3 3
vesæl 11. The dry additives can be added in this method even if the reagent is introduced
by other known methods.
F.Y~mples of dry additives 36 which could be added to promote oxidation within the
~ abso~ vessel 11 include compounds of iron, m~n~n~se; v~n~ lm an~other~metals that
5 promote or catalyze oxidation.
Examples of dry additives 36 which could be used to e~h~nre chemical absorption
of the S2 within the absorber vessel 11 include m~nesium oxide, ammonium hydroxide,
sodium carbonate, sodium sulfite, sodium hydroxide, m~n~sil-m sulfite, and other soluble
aLkali compounds of m~n~sillm~ ammonium, pot~ssillm~ calcium, and sodium, used to
10 enh~nr~ absorption in a calcium (limestone or lime) based FGD system.
Examples of dry additives 36 which could be used to provide a desired degree of
burr~.hlg to the desu!furization process occurring within the absorber vessel 11 include
sodium fo~ , dibasic acid (DBA), sodium citrate, adipic acid, succinic acid, and other
organic acids and/or their solid colL~poullds including formic, acetic, hydroxypropionic,
15 sulfosuGr-inic, adipic, phthalic, benzoic, fumaric, hydroxyacetic, succinic, and lactic.
F~ s of dry additives 36 which could be used to inhibit oxidation to reduce scale
growth within the absorber vessel 11 include coul~oullds of formate and thiosnlf~ and
el~m~nt~l sulfur.
An ~Y~.IIplr- of a dry additive 36 which could be used to promote or specify the type
20 of or degree of cryst~lli7~tion, etc. in the desulfuri_ation pl~cess occurring within the
absGll~r vessel 11 is polysulfonate.
As the examples Listed above in(~ir~t.q., some of the various dry additives 36 can
~)lOLU<~k: more than one kind of desired activity within the absorber vessel 11. For eY~n rle,
sod~m formate has been shown to inhibit oyi~tion and provide l UlLlldlS; ions to buffer and
25 ~l~LuO~ SO2 removal in r~lrillm based FGD ~ms. Also, additives such as iron EDTA
can be used to plOLuo~ removal of nitrous oxides in a flue gas desulrll. ;~ion system. It
wiU also be a~l~id~ that more than one dry additive 36 could be employed at the same
time, i.e., two or more dry additives 36 could be ~ lly injected into the absoll3el
vessel 11 via the q~ air ar1<liti~n system, so long as the two or more dry additives do
30 not ploduce an adverse .~ l reaction th~wæL~, or upon the ~esnl r~ ;on ~r~cess

` - 216S~33
CAS~ 5580
occurring within the absorber vessel 11. By way of example and not limitation, the dry
additives sodiurn formate and sodiurn thiosnlf~t~, or calcium carbonate and DBA, could be
pn~ lly injected simlllt~nfously without adverse effect. However, combinations of
u~.iron and thiosulfate, or sodium formate and DBA for example, would not be;desirable
S because the first combination ,e~resellls opposing goals of promoting and inhibiting oxidation
while the second is not desirable because the two additives are used to accomplish the same
goal of l~urr~ g.
While the solids pick-up point 32 can be located at virtually any point in the line 26
dc,w~l~ll of the oxidation air supply means 25, it is preferable to locate it as close to the
absorber vessel as practical. This will minimi7~ the length of line 34 and the associated
additional ~res~ulc: drop and abrasive wear due to the solids conveying function. Sirnilar
location considerations would apply to any sep~ate dry additives 36 pneumatic conveying
pick-up points 38, 39. l\~finimi7.ing the number of bends and line direction changes in line
34 will also serve this end.
Multiple system design configurations and arrangements are also possible. Through
the use of the present invention, each individual overall FGD system design may be adapted
for use with the present invention, even uniquely designf~l and e-nginf~ered arrangements,
equipment selections, and configurations. An exarnple of one such variation is illustrated
in Fig. 2.
Rf f~ g to Fig. 2, the system 40 l~ceivt;s dry reagent 12 through line 16, either by
~llfY`~ conveyallce, or by dilute or dense phase pl~f~..l.~ti- conveyance, in order to be
stored in surge bin 14. A rotary airlocl~/Ç~der 42 provides both the airlock and feed rate
control function to supply the dry reagent 12 through chute 44 to oxidation air line 26 at
pick-up point 32. I~e solids and air mix~re is then collv~d di~ly through a straight run
25 of pipe 46 to an injection point or points 48 located within an absorber reaction tank or
vessel 50. n~ f s or mllltiple alla~g~ can be configured in order to ~cr~ase theu~~ y of injection points 48 as l~uh~d by the FGD process. If desired, injection point
or points 48 can ~ e in a ~/i,i~ily of a pln,~ flow discllarge from a m~.l-
~
agitator 52, for lli~ .~;on of both o~iA~tinn air stream 24 and reagent 12 into the absofl~l30 reaction tank or vessel 50. To f~rilitslt~ other possible arrangements, t~he reagent flow

CASE5S80 216S633
control function could be provided remotely, wllel~y the dry reagent 12 is either dilute or
dense phase ~ lly conveyed, from a remote location, directly to the oxidation air
line 26 solids pick-up point 32 at the desired rate. This would allow the feed rate of the dry
reagent addition into the absorber vessel 50 and the feed rate of the oxidation air stream into !i.
5 the absorber vessel 50 to be independently controlled. In either case, the oxidation air line
26 solids pick-up point 32 should be provided at an elevation above a slurry liquid level 56
in absorber reaction tank 50, so that if the air supply means 25 fails, the slurry 54 will not
back-up into the e~ "~ piping 26, 44 located at or above the elevation corresponding to
the liquid level 56. Additionally, a lllillill""" feed rate of the oxidation air stream 24 would
10 usually be supplied whenever the feed rate of the dry reagent 12 is greater than zero, to
prevent solids dropout in the piping 26, 46.
Variations in the dis~ ing means 52 used to disperse the solids-air mixture into the
slurry 54, such as by the use of modified sparge headers, injection lances, jet
mixers/aerators, etc., can also be applied as deemed applicable to the overall process.
The process accoldillg to the present invention can reduce overall plant capital costs
by incorporating portions of the fresh reagent feed functions and the oxidation air addition
filnrfion~ into a single piping system. If a dry grinding system is required on site, it might
draw more power then a colllpalable wet grinding system. However, this could be off-set
by the lack of recycle water piping from a dewatering system to a reagent ~,~al~lion
system, reduced recycle water pump sizes, increased slurry solids den~itilo-s throughout the
plant and by the lo~ ing of hydraulic loadings throughout the plant.
The ~ invention allows increased FGD ~Irol~ce in the absorber reaction
tank 50 due to a higher slurry solids density. The present il~ ioll also eli.~ t~ the need
for fresh slurry feed pumps and associated slurry supply loops.
2S Additionally, the present invention provides for a r~llrtion in the size of the fresh
reagent surge storage vesæl; it also ~ tes the ~otelllial for reagent powder carryover
from the absoll,c. ~ ion tank 50 since the reagent is introduced below the liquid level 56
therein, rather than clæwll~, within the absorber reaction tank 50.
The ill~t;~i~ll can be used to ~rr~ively introduce a wide varie~ of reagents into the
absorber, such as the ~ lk~lin~ reagent, as well as various dry additives such as

- 2165633
CAS~: 5580
oxidation promoters, b~fr~ g agents, etc. Accordingly, while a specific embodiment of the
invention has been shown and d~-il,ed in detail to illustrate the application of the principles
of the invention, it will be understood that the invention may be embodied oth~L ~ise without
departing from such principles.- Such embodiments have been omitted herein for the sake
5 of conciselless and readability but properly fall within the scope of the following claims.

Dessin représentatif
Une figure unique qui représente un dessin illustrant l'invention.
États administratifs

2024-08-01 : Dans le cadre de la transition vers les Brevets de nouvelle génération (BNG), la base de données sur les brevets canadiens (BDBC) contient désormais un Historique d'événement plus détaillé, qui reproduit le Journal des événements de notre nouvelle solution interne.

Veuillez noter que les événements débutant par « Inactive : » se réfèrent à des événements qui ne sont plus utilisés dans notre nouvelle solution interne.

Pour une meilleure compréhension de l'état de la demande ou brevet qui figure sur cette page, la rubrique Mise en garde , et les descriptions de Brevet , Historique d'événement , Taxes périodiques et Historique des paiements devraient être consultées.

Historique d'événement

Description Date
Le délai pour l'annulation est expiré 2015-12-18
Lettre envoyée 2014-12-18
Inactive : TME en retard traitée 2003-12-03
Accordé par délivrance 1999-05-18
Inactive : Page couverture publiée 1999-05-17
Inactive : Taxe finale reçue 1999-02-16
Préoctroi 1999-02-16
Lettre envoyée 1999-01-15
Un avis d'acceptation est envoyé 1999-01-15
Un avis d'acceptation est envoyé 1999-01-15
Inactive : Renseign. sur l'état - Complets dès date d'ent. journ. 1999-01-11
Inactive : Dem. traitée sur TS dès date d'ent. journal 1999-01-11
Inactive : Approuvée aux fins d'acceptation (AFA) 1998-11-19
Demande publiée (accessible au public) 1996-06-20
Toutes les exigences pour l'examen - jugée conforme 1995-12-18
Exigences pour une requête d'examen - jugée conforme 1995-12-18

Historique d'abandonnement

Il n'y a pas d'historique d'abandonnement

Taxes périodiques

Le dernier paiement a été reçu le 1998-12-11

Avis : Si le paiement en totalité n'a pas été reçu au plus tard à la date indiquée, une taxe supplémentaire peut être imposée, soit une des taxes suivantes :

  • taxe de rétablissement ;
  • taxe pour paiement en souffrance ; ou
  • taxe additionnelle pour le renversement d'une péremption réputée.

Les taxes sur les brevets sont ajustées au 1er janvier de chaque année. Les montants ci-dessus sont les montants actuels s'ils sont reçus au plus tard le 31 décembre de l'année en cours.
Veuillez vous référer à la page web des taxes sur les brevets de l'OPIC pour voir tous les montants actuels des taxes.

Historique des taxes

Type de taxes Anniversaire Échéance Date payée
TM (demande, 2e anniv.) - générale 02 1997-12-18 1997-12-01
TM (demande, 3e anniv.) - générale 03 1998-12-18 1998-12-11
Taxe finale - générale 1999-02-16
TM (brevet, 4e anniv.) - générale 1999-12-20 1999-12-02
TM (brevet, 5e anniv.) - générale 2000-12-18 2000-12-01
TM (brevet, 6e anniv.) - générale 2001-12-18 2001-12-03
TM (brevet, 7e anniv.) - générale 2002-12-18 2002-11-29
TM (brevet, 8e anniv.) - générale 2003-12-18 2003-12-03
TM (brevet, 9e anniv.) - générale 2004-12-20 2004-12-02
TM (brevet, 10e anniv.) - générale 2005-12-19 2005-12-02
TM (brevet, 11e anniv.) - générale 2006-12-18 2006-11-30
TM (brevet, 12e anniv.) - générale 2007-12-18 2007-11-30
TM (brevet, 13e anniv.) - générale 2008-12-18 2008-12-01
TM (brevet, 14e anniv.) - générale 2009-12-18 2009-12-01
TM (brevet, 15e anniv.) - générale 2010-12-20 2010-11-30
TM (brevet, 16e anniv.) - générale 2011-12-19 2011-11-30
TM (brevet, 17e anniv.) - générale 2012-12-18 2012-11-30
TM (brevet, 18e anniv.) - générale 2013-12-18 2013-12-02
Titulaires au dossier

Les titulaires actuels et antérieures au dossier sont affichés en ordre alphabétique.

Titulaires actuels au dossier
THE BABCOCK & WILCOX COMPANY
Titulaires antérieures au dossier
DENNIS WAYNE JOHNSON
KEVIN JOHN ROGERS
Les propriétaires antérieurs qui ne figurent pas dans la liste des « Propriétaires au dossier » apparaîtront dans d'autres documents au dossier.
Documents

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Liste des documents de brevet publiés et non publiés sur la BDBC .

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Description du
Document 
Date
(aaaa-mm-jj) 
Nombre de pages   Taille de l'image (Ko) 
Revendications 1998-10-27 4 159
Description 1996-04-29 8 388
Revendications 1996-04-29 5 191
Dessins 1996-04-29 1 14
Abrégé 1996-04-29 1 16
Dessin représentatif 1999-05-10 1 4
Dessin représentatif 1998-03-18 1 6
Rappel de taxe de maintien due 1997-08-18 1 111
Avis du commissaire - Demande jugée acceptable 1999-01-14 1 163
Avis concernant la taxe de maintien 2015-01-28 1 170
Correspondance 1999-02-15 1 45
Taxes 1998-12-10 1 32
Taxes 1997-11-30 1 28
Courtoisie - Lettre du bureau 1996-01-28 2 57
Demande de l'examinateur 1998-08-24 1 36
Correspondance de la poursuite 1995-12-17 88 4 585
Correspondance de la poursuite 1995-12-17 22 956
Correspondance de la poursuite 1996-11-11 1 26
Correspondance de la poursuite 1998-10-12 2 54