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Patent 2131987 Summary

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(12) Patent Application: (11) CA 2131987
(54) English Title: METHOD FOR REMOVING SULFIDE WITH CATALYTIC CARBON
(54) French Title: METHODE POUR ELIMINER LE SULFURE A L'AIDE DE CARBONE CATALYTIQUE
Status: Deemed Abandoned and Beyond the Period of Reinstatement - Pending Response to Notice of Disregarded Communication
Bibliographic Data
(51) International Patent Classification (IPC):
  • B01D 53/34 (2006.01)
  • B01D 53/86 (2006.01)
  • B01J 21/18 (2006.01)
  • C01B 17/04 (2006.01)
  • C01B 32/336 (2017.01)
(72) Inventors :
  • HAYDEN, RICHARD A. (United States of America)
(73) Owners :
  • CALGON CARBON CORPORATION
(71) Applicants :
(74) Agent: BORDEN LADNER GERVAIS LLP
(74) Associate agent:
(45) Issued:
(86) PCT Filing Date: 1994-01-21
(87) Open to Public Inspection: 1994-08-04
Examination requested: 1994-10-20
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/US1994/000884
(87) International Publication Number: WO 1994016990
(85) National Entry: 1994-09-13

(30) Application Priority Data:
Application No. Country/Territory Date
008,723 (United States of America) 1993-01-21

Abstracts

English Abstract

2131987 9416990 PCTABS00033
An improved process is provided for the selective removal of
sulfide from gas or liquid media containing oxygen and water by
contacting said media with a catalytically-active carbonaceous char.
The improvement is provided by the use of a catalytically-active
carbonaceous char prepared by low-temperature carbonization and
oxidation of a bituminous coal or bituminous coal-like material
followed by exposure to a nitrogen containing compound at
high-temperatures during the initial calcination and/or activation of the
oxidized material.


Claims

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


WO 94/16990 PCT/US94/00884
AMENDED CLAIMS
[received by the International Bureau on 16 July 1994 (16.07.94);
original claims 1, 2, 5 and 6 amended; original claim 3 deleted;
new claim 7 added; remaining claim 4 unchanged;
claims renumbered 1-6 (1 page)]
1. A process for the removal of sulfides from gas or
liquid media which comprises contacting said media, in the
presence of oxygen and water, with a catalytically-active
carbonaceous char, said char being prepared from a bituminous
coal or a coal having bituminous properties carbonized and
oxidized at temperatures below 700° C and subjected thereafter
to nitrogen-containing compounds while heating to temperatures
greater than 700° C.
2. A process as set forth in Claim 1 wherein said
catalytically-active carbonaceous char has been activated at
temperatures above 700° C using at least one of steam, carbon
dioxide, and oxygen.
3. The process of Claim 1 wherein the sulfide is hydrogen
sulfide.
4. The process of Claim 1 wherein said process is operated
at a temperature of between 0° C and 300° C to remove said
sulfides.
5. The process of Claim 1 wherein said process is operated
at a temperature of between about 25° C and 90° C to remove said
sulfides.
6. A process as set forth in Claim 1 wherein said
nitrogen-containing compounds are urea and nitrogen-containing
compounds having at least one nitrogen-containing functionality
in which the nitrogen exhibits a formal oxidation number less
than that of elemental nitrogen.

Description

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


' WO 9411C990 2 1 3 1 9 8 7 PCT~S94/0088~
..~
. . .
- Tm,~e -~ :
,
MET~IOD FOR REMO~XNG SUL~IDE WIT~ CATALY I IC G~RBON
LD OF T~E lN~FNllON `; ` ` ~ ` `
Thc p~sent i~lVCDtiOD ~elates tO thc USC of a higSly colybcDlly ~ c c~s char for Ihe
E~ rcmoval of sulfJdc ~om gâs~or~q~d media ~ osencc dODCygeD and~wa~cr. `' `~ :^ i
:: BACKG~OU~DOFT~IN~'ENlION ~ ~ ~
VJ~rious mc~ of rcmo~ing H~S using a~s~ re hwwo. For e~ple, 1~ ~as been
uscd for the ~emoval of hydFogcn ~ulfidc and vl~rious mn~sn~ a humidifiod, ~ng
10 gas~ous stream. ImptovemeD~s in thc~vai qrbilibe~ of ~l# C~35 ch~ hvcbccD realized by
the addi~ion of a basc~ such as ~nunonia or hydroxi~ to tbc char w~c d~g the~:mov~;psocess. It
hasbeenf~undths~ ~dditionofc~l-inhalogens~Dd~ransido~c~ali~c~schar
substratcs also the l~movd of hydioge~ nd m_ ~m ~d air ~ums. Howcvcr,
noneoftheseimplovcmu! ~edtheirhe~tplopQticsd~ ~entally
1 ~i responsible for lhe obscrvcd pbawmalon in the abscncc of promo~ wch as ~ y~idc, potassium
iodide, or othcr compuulds. : :
Some implovcments iu thc po~e ~ze distribudon of ~cdvu~ cub~s hllve beeD dcsc~ibed wherein
a high-~cm~alre cdvued cubon~ char is ~led~with ~ or mel mi~compwnd~and calcineda~high~ es. ChucFc~dinthis~m n~erhav~eD~edbyd~a~ biDdes;
20 bowever,: the ~ili~ of such chan to ~emo~c h~ u~lfidc by c~lytic <~do~ was not ~ or
~: ~eported. l~çptoductiond~c~uschar~ ~btbkf~chy~genwlfidco~cnhasbeeR~aught whclein a high-temp~#~re aeti~ bon colce i~ o~idi~d ~nd e~ed to a ni~conu~ning
ammoruum salt al tcmpo~res abo~c 3S0 C.

wog41l6g902~31987 ~ . ;; PCT/US94/00884
Such prior an methods have c~rlain disadvantages which limit ~hcir applicaioa. The usc of
commercially-availablc unimprcgnatui scdvn~cd carbons for cataly~ic hydroger1 ~utfide remova~ suffers from
low rates of aemo~ral, ~nd conscqucntly, low hydrogc~ sulfidc b~a~through c~citics. T~c u5c of promotc~s
in the p~escncc of ~2ch ~naceous ~s also entails cerlain di~advantagcs. For c~amplc, thc use of
5 ammonia roqlai~s added cost and ha~ard in thc ~ns~ion al~d co~trol ~3f measmed a~monia additio~. The
usc of sodium hydm~ide a~d o~er mc~al ul~ ~Iso iD~rolva addcd costs ~ ~ell as ~ iDc~ascd dsk of
thennal cxcursjo~ d~c to the 3Owenng of the char ignition tempcsa~e.
Accordin~ly, it is Ihe o~joct of ~hc p~e~t i~vention to p~dc ~ cut~ c~u which iscataly~ically activ~ for sulfidc and me~csptan removal in thc presencc of o~ygeD aDd water wbcl~ compased
10 to other unimprcgDated chars and ap~ *om t~se ac~ic parame~ h~own to affect ~ch removal. For
cx~mplc, c~t insic p~uamete~ ca~ includc p~ticlc size di~ributioD, po~ volumc distJibudoo, and contact
~ime. It ~s further thc object of thc p-e~ent iovendon to produce a~d employ ~uch ~onsc~s chars at
minimal cost ~nd hazard when comp~ed to pnor ar~ .
~ . . . .
SUMM~RY OF T~IE INVENlrlON
., I :`
Gcncrally~ the present inven~on co2np~scs the ~:moval of w~ldcs aDd mc~aptans from media
containing oxygen and watcr by thc cataly~c action ~f aubonacoous chars. l~cse c~ars arc prcparcd by
the low-tem~rc carbonization and oxitation of nit~cn p~r feedstocl~ Thc o~idizcd low-
temperature c~ar is Ihcn subjected to a nitroge~tai~ng ~p~und at high tempa~res during thc initial
~alcination or calcination/acd-ation. Ln all cascs, bightall~ c~w cha~ re those p~aduced
20 by ~hennal ~mcn~ at tempa~tures gralterthan 700 C Low ~pC~E cubonacoous ch~ are those that
havc no~ aspenenccd tempe~res ~ate~ Ihan 700 C.
The prefe~d ~trogen-~ feodstoclt i- a bi~minou~ coal or a bi~miwus co~l-lilce ma~ial such
as thosc dcrivod from higher or loweT ~nlc bi~meDs, coals. or lipoocllulo~c m~ by various ehunical
Iseatments. B~amples of higher ~ ooals include ~th~acite or scmi~ c coals, while c1samples of
25 lower ranlc coals include peatt lignitC~ and sub-bi~mi~ous oo~ls. E~amplc~ of lhe ehemieal treatment of these
fecdstocks include all~ali metal trea~mcnt of thc high ~anlt ~ial6 aDd ZiD: chloride or phosplloric æid
trcatment of thc low ~anlt matcrials. These typcs of treatmc~ts can slso be ~pplicd to lignocellulose matenals.
. . .

WO 94116990 2 1 3 1 9 8 7 ~ ; ~/US941008~
In a prcfened embodimcnt of llbi8 iDvention, thei feedstocl~ matsrial i~ aizcd, mixcd if necessary
with small alslounts of a suitaUc binder such a~ pitch, briqucucd or o?Lherwiisci fonned, and sizcd. Thc sizcd
matcnal is ?Ihen cxtensi~dy oxidized at tcDlpcrah~rcs Ics~ ~han 700 C, prcfe~ably les?ic than 400 C. The
5 oxida~ion is continucd UDlil additioDal ga D the catalytic acti~i~ty of thc fiDal prot?ua U~c 1~0 IOlSger eviden~.
Thc oxidation i c wcll bcyond lhat ~ically required to r~s~ove lhc col~ng proper~ of bi~ coals and
pr~uces an optimally o~cidized ch~. Otl~e~ oo~vel icnt mcaD~ of o~ on c~ d60 be usod to cf~eGt thc
low-tempe~ re oxidatioG and c~bonizatio~ of thc ~K m~ s ~:
~e oxi~zcd low-tcmp~re c~ char i~ thc~ a~po~ed to ~iall ~nounl~c of ~n
10 inexpe~ciYe~ abundar~ ~d sclativcly ~-toxic nilrogc~-contai~iDg compou~d ~uch as urca du~ing, no~ ahcr,
thc initial calcination and co~on of she aubon ~ Thc amo~t~ of nilrogen-con~aiDing
compounds uscd ase typically w~all, prcfe~ably Icsc tb~ S% by wcight of thc o~idizcd b~mpc~re
carb~nacoous char`or ~uch ~ ddido~l guns i~ th~ cs~y~c ~tiv,ity Qf th~ al ~UCI `aré~no longer
cvidcnt. Thc t-eatm_ is ca~Ti~ b~i hea~ng t} o~i~ rc char to bigh temp~res,
15 ~prcferably belween 8S0 C and 9S0 C, in the p~e of t~e nilrogen~onuining comp~nd. This hc~ting is
preferably conductc~ undcr an ~mo~pherc Ibat is inert accept ~orthc ~asa and vapors atlributablc to the ch~r
andfor the nitrogcn-containing compowld. The bcasin~ e and ~p~ efe ably selccscd such
that addhional ~ns i~ the catalytic cti~iq of ~c final product l~se oo ~gcr cvidcnt. ~ ~
Thc nitrogcn~ ed high-tem~ c us cbt~r may then bc acdvated to ~hc desired
20 density at tempera~res sbove 700 C in ~tcam andfor c~bon dio~ nth or without thc addidon of otbcr
gasifying agents wch as alr. Thc calcincd or calcined/acti~ated c s char is then cooled in an
- oxygen-frce or olhe~wisc iDCrt ~Itmospberc to tempc~ Ic~s tbaD ~ C, p~fe~ably Icss thar 200 C.
Additional gains in alalylic actiYiq may bc ~lizod blr epcating t~c o~udation~ powrc lo nitrogcn-
conlaini~g compouDds~calcina~on or calcin~tionf~lctiY~ Dert coding as m~my tuncs as may bc desircd.
25 Altcrna~iYely, any o~h~ mcthod ~ to genale cataly~ic ~iviq in high tempQ~e c~ceous chars
may be applied IO the rcsultana product to fb~thar ~DhaDcc its a~talytic ~ctivity.
The cataly~c~y-utive c~ char p~d ~ocdLng to the above method is then contac~ed
with a sulfide~ontai~g media in the prescnce of watcr ant o~ygen. Sulfide is rcmoved f~om the media by

wo 941l69go2~.3 19 8~ Pcr/usg4/oo~
calalytic oxidation to primalily sulfates and clemen~l ~ ur. The o~ng tcmpuaturc is b~wecn ~1s ~1t
O C and 300 C and pseferably bcswecn about 0 C and 100 C and morc preferably b~w~en about 2S C an~ 90
C.
PRESENTLY ~FERRED EMBOD~ENTS i -
~; lheutili~o~ein~endo~isillustra~dbythefollo~qngtwoex~mple~. Incache%ample,oquivalent
mcsh sizc fmctions of thc ca~bonaceous c~s wcrc evsl~cd t4 ~cgate any particlc sizc effec~ Thc chars
used in thesc examples ha~e appFo~y the ulmc de~e~ and CCI, acdvities. Tbi~ Deat oguivalcnce
indicates that the porc volumes of both chan ue nea~ly equivalen~ Thc~eforc ~c bcncfits of ~e prescnt
i nvcntion ~rc cvidcnt as thc extrinsic propefie~ affccting clllfidc ~mt>val ue nc~rly oqui~alent for thcsc
10 samples. E~ple 1 temo ~hcH2Sremovalapaci~ofa~pcndcmesh~f~ionofacommacial
. .." -"~ actiYa~ed ca~on. Examplc 2 dcmonstr~cs the 1~2S Doval capaciq o~he invcndon. Companson of lhesc
. , .-two examples shows ~hat the perfonnance of the invendon grcady e~cceeds that of a typical acti~/atcd carbon.
~ -:
EXAMPLE 1 ~ . ~
A commerci~lly available sctivaled aubon, 8PL (~d by Cslgon CSUbOD Co~oration,
15 Pittsburgh PA~ was sizct to less than S ~ g~er than 6 mcsh (IJ.S. St ndard Serics sieYcs). When ~o sized
this carbon showed an Apparent Density ( Test Method TM-7, Calpn Carbon Cpo~ion, Pi~sburgh PA)
of OrS04 gTams per cc and a ca, Nwnber ( Tesl M~ TM-6, Calgon Cllrbon Corpo~ation, Pitlsburgh
PA ) of 55.1%. The sizcd carbon was loadcd inlo a ~lum- having ao insite diamaer of ~ppro~umately 0.73
inches to gi fe a bcd depth of 9 inchcs. Column lo ding w~ done in ~uch a manneras to achieve a packinn
2Q density cquivalent to ~c Apparcnt Dalsity. A ~as strcam ba~g ~ relativc humidity of g~er than 50~fc,
an oxygen content of g~ea~ than 17 vl~f*, and a howo H2S concenllYion of app~im~y I vh/% was
passed through this eolumn al a flow rate of 1~50 ~ ~tc und ambicn~ dîdons. The cfflucnt
from this column was monito~ nd the el~l time re~ui~d to chieve a 50 wm H2S breal~luough was
measured. For this ea~on sample the elapsed timc piod w~s equal to 9 mi~utes.

~1~198~
WO ~4116990 ^ PCT/US94/008~4
. EXAMPLE 2
Bituminous coal was pulvaized, mLl~ed with ~ut 4 tc 6% coal t.ar pitch, and briquctIcd. The
rcsul~ant briqueues were crushed and sized to producc ~ appro~imatcly less than 4 mcsh size and greatcr
than 10 mesh sizc (U.S. Slandard Se~ies devcs) maserial. ID thc prcsc~cc of largc quan~ tics of e~ccss air,
this material was o~idized by hcating from 100 C to 200 C a~ a ~ate of 200 C pcr hour, thCD from 200 C to
350 C at a rate of 100 C pa hour, then held at 3SO C for 4 ~ and fi~ally h:atcd from 3SO C to 450 C at
- a ratc of 100 C per hour. The rcsult~nt o~cidi2ed matcrial was coolod to Dear ambicnt tcmp~us~s în a low
o xygen content a~mosphere, sizcd to produce an #pp~o~atcly lc~ ~ S ~nd gteater Iban 6 mcsh ~izc (U.S.
Slandard Scrics si~res) n~serial, and ~ubscqucntl~ imprc~ with an aqueous ures soludon and dricd. Thc
10 ~uantity of urca ~oludon u~sed was sufficic~t to producc a 4% urea loading o~ a dry wcigh~ b~sis. Aftcr
impregna~ion,portionsoftheo~udized,imp~ atedlow-~paaturccharwacrapidlybcatedto950Cunder
. an incrt gas atmosphere. ~cdia~ely following this calcina~ion ~ nent thc resultant ma~erials wcre
zctivaled with stcam at 950 C for a ~uffi~c~t pcriot of timc to acbievc ~he dcsired yidd. After activation,
the materials werc coolcd ~o ambicnt ~em~ under a~ iDert ~plleYc. The catalyticaliy-aclive
15 ~ ivated ca~bonaccous chars ~o prQduccd, when combincd and dzed to less ~an S mesh (U.S. Standard
&!~ies) and greater ~ 6 mcsh (U.S. St~ Scnes) exhibitot ~n Ap~t Dcnsity ~cst Mcthod TM-
7, Calgon Car~on Colporation, Pittsburgh PA) of 0.49S g~ams per cc. Thc CC:I, Numbcr of the sizcd,
combincd chars was SS.S%.
Thc H2S rcmoval ability of thc sizcd, catal~tically-~lc~ivc, activatcd high-tcmpcraturc carbonaceous
20 char prepared as described above was ~inul using conditions idcntical to thosc describcd in Example
1. For tbis sample of catalytically-activc activatcd car'oonacoous char the elapsed time pcriod ~cquired to
achicvc a SO ppm H~S brcalcthrough was oqual to 326 minutcs.
While a prescntly prefe~ed embodiment of thc invcntion ha~ bCeD dcscribed, it may be otherwisc
cmbodied within the scopc ~f tllc appeDded claims.

Representative Drawing

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Administrative Status

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Event History

Description Date
Inactive: IPC deactivated 2017-09-16
Inactive: IPC from PCS 2017-01-07
Inactive: IPC expired 2017-01-01
Inactive: IPC from MCD 2006-03-11
Inactive: IPC from MCD 2006-03-11
Inactive: IPC from MCD 2006-03-11
Application Not Reinstated by Deadline 1996-07-21
Time Limit for Reversal Expired 1996-07-21
Inactive: Adhoc Request Documented 1996-01-22
Deemed Abandoned - Failure to Respond to Maintenance Fee Notice 1996-01-22
Request for Examination Requirements Determined Compliant 1994-10-20
All Requirements for Examination Determined Compliant 1994-10-20
Application Published (Open to Public Inspection) 1994-08-04

Abandonment History

Abandonment Date Reason Reinstatement Date
1996-01-22
Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
CALGON CARBON CORPORATION
Past Owners on Record
RICHARD A. HAYDEN
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) 
Abstract 1994-08-04 1 49
Cover Page 1994-08-04 1 56
Drawings 1994-08-04 1 29
Claims 1994-08-04 1 53
Descriptions 1994-08-04 5 348
Prosecution correspondence 1994-10-20 1 19
Courtesy - Office Letter 1994-10-20 1 16
International preliminary examination report 1994-09-13 2 44