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KYUSHU
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rce Science
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Edited by:
Sudarto Notosiswoyo Hideo Nagashima Kikuo N/atsui Budi Sulistianto
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Proceedi The
ZndEa
Joint
March
10 - lnstitutBandung,
I."4.
lti
I
Proceedings of
The Znd lnternational Symposium of Novel Carbon Resource Science
Earth Resource Science and Technology
Joint Symposium
Kyushu University-
lnstitutTeknologi
BandungMarch 10
-
11, 2009lnstitut
Teknologi
Bandung (lTB) Bandung, lndonesiaEdited by:
Sudarto Notosiswoyo
I nstitut Teknologi Bandung, lndonesia
Hideo Nagashima
Kyushu Universi$, Japan
Kikuo Matsui
Kyushu U niversity, J apan
Budi Sulistianto
lnstitut Teknologi Bandung, lndonesia
Proceedings of
The 2no lnternational Symposium
of
Novel Carbon Resource ScienceEarth Resource Science and Technology
Joint Synrposium Kyushu University
-
lnstitut Teknologi BandungMarch, 2009
Technical editors:
Nuhindro P. Widodo (lTB) M. Nur Heriawan (lTB) Akhmad A. Korda (lTB)
International Symposium of Novel Carbon Resource Science (!ud; 2009 : Bandung)
Proceedings international symposium of novel carbon resource sciences : earth resource
science and technolory March 10-11, 2009 ITB Bandung / edited by Sudarto Notosiswoyo...
[et.al.l. -
-
Bandung: Fakultas Teknik Pertambangan dan Perminyakan ITB, 2009.395 hlm. ; 2.3 cm.
ISBN 978-979-8305-30-6
1.
IGrbon--
Kongres.II.
Sudarto Notosiswoyo.Printed by:
Faculty of Mining and Petmletrm Engineering Institut Teknologi Bandung
JI. Ganesa 10 Bandr:ng 40132 lndonesia
I. Judul.
662.930 6
CONTENTS
PREFACE CONTENTS
KEYNOTE PAPERS
1.
MODELING AND REMEDATION WITH PERMEABLE REACTTVE BARzuERS IN GROUND WATER CONTAMINATED B Y PERC HLOROETFryLENEYanqing WU
2.
CATALYTIC EFFECTS OFALKALI
ANDALI(ALINE
EARTHMETALLIC
SPECIES DURING TTIE GASIFICATION OF BROWN COALChun-Zhu
Li
3.
COAL GASIFICATION AND LIQUEFACTION: A BRIEF REVIEWDwiwahju Sasongko
4.
DEVELOPMENT OF ECO.FRIENDLY COAL MINES IN OVERSEAS COUNTRTES CONSIDERING ENVIRONMENTAL IS SUESKikuo MATSUI
5.
TWO MAJOR PROBLEMS OF CO2-ECBM PILOT TEST PROJECT AT YUBAzu, JAPAN6. Low
RANKcoAL ,'GRADING
Kvuro SASAKIBukin Daulay
I.
COAL RESOURCE UTILIZATION
I.I.
UPGRADING OF LOW RANK COAL AND WOODY BIOMASS BY I{YDROTHERMAL TREATMENTTsuyoshi HIRAJIMA and Moriyasu NONAKA
1.2.
PRODUCT CHARACTERIZATION OF RAW PEAT AND LOWQUALITY
COAL TREATED BYALI(ALINE
HYDROTHERMAL: A NOVEL METHOD OF COz CAPTURING AND HYDROGEN GENERATIONAnggoro Tri MURSITO, Tsuyoshi HIRAJIMA and Keiko SASAKI
1.3.
COAL BASED LATERITIC TRON ORE REDUCTION: KINETIC ANALYSISSoepriyanto, S. , Nababatr, M., and Pramusanto
1.4.
STUDY OF LOW RANK COAL GASIFICATION PROCESS BY FLUIDIZED BED GASIFICATIONEdy SANWANI, Ikhsan SEPTI.ANSYAH, Arief SUDARSONO, Ismi
HANDAYANI
II. EARTH RESOURCES
2.1.
DIFFERENCES IN THE GEOSTATISTICAL AND GEOLOGICALCHARACTEzuSTICS OF COAL SEAMS FROM KUTEI AND SOUTH SUMATRA BASINS _ INDONESIA
Chairul NAS
2.2.
PETROGRAPHY OF CARBONIZATION INTHERMALLY
METAMORPHOSED COAL FROM TANJTJNC ENIM AREA, SOUTH SUMATERA BASIN, INDONESI"AD. Hendra
AMIJAYA
llt
I-1
I- 10
I-18 125
II-1
v
4
6
8
V
II.1 O
1
l9
25
2,3
SPATIAL CHARACTERIZATION AND GEOLOGICAL MODELING OFI{ETEROGENEOUS RESOURCE QUALITY IN A MULTILAYER COAL DEPOSTT Mohamad Nur HERLAWAN and Katsuaki
KOIKE
2,4. MAGING
OF COAL NEAR SUBSURFACE INTRUSION BODY THROUGH SEISMIC TOMOGRAPTIY: A CASE STUDY IN SUBAN BLOCK MUARA ENIM SUMATRABagus Endar B. NURHANDOKO, Budi SULISTYANTO, SYAFRIZAL, Y. WTYANTO, Hussein RUDryANTO, M. Puput ERLAI{GGA, Erwin RIYANTO, Danang KUSUDIHARJO, Fajril AIVIBIA
2.5.
REMOTE GEOLOGICAL MAPPING IN TARHLINAH AREA,LIBYA
Nureddin M. SAADI and Koichiro WATANABE
III. COAL MINING SCIENGE AND TECHNOLOGY
3.1
APPLICATION OFA
PLINCH MINING SYSTEM TO INDONESIAN COAL MINES Hirotumi FURUKAIVA,Kiluo
MATSUI, Takashi SASAOKA and Hideki SHIMADA3.2
ESTIIvIATION OF ANI OPTIMUM STZE OF BLASTED ROCKS USING POWDER FACTORAI{D
DIGGING RATE DATA: A CASE STUDY AT BENGALON PIT A, BENGALON COAL PROJECT, EAST KALMAI.{TA}.I, INDONESIAGanda M. SIMANGUNSONG, Obes B.H. SILALAHI, Suseno KRAMADIBRATA, and Beni RASJID
3.3
SOFT ROCK BEHAVIOUR WITH PARTICULAR REFERENCE TO COAL BEARING STRATASuseno KRAMADIBRATA, Singgih SAPTONO, Yudhidya WICAKSANA, Simon H PRASETYO
3,4
DEFORMATION MONITORING AT LOW-WALL SLOPE OF COAL OPEN PIT IN PT.ADARO, INDONESIA
Budi SULISTIANTO, Suseno KRAMADIBRATA, Ridho K WATTIMENA, Singgih SAPTONO, Patrno NUGROHO
3.5 A
STUDY OF BLAST VIBRATION INDUCED FRACTURE IN LIMESTONE QUARRYSugeng
WAftfUDI,
Takashi SASAOKA, Hideki SHIMADA, Kikuo MATSUI3.6
NUMERICAL SIMULATION OF DIFFUSION IN MINE AIRWAYS USING DISCRETE TRACERMOVEMENT METHOD AND EFFECT OF DEAD SPACES AREAA. WIDIATMOJO, K.SASAKI, N.P. WIDODO, G. ARPA, Y. SUGAI
3,7
NUMERICAL MODELING OF DMFUSION PHENOMENA IN NARROW VEIN MINE STOPE FROM FIELD MEASUREMENT AND SCALED LABORATORYGabriel ARPA, Kyuro SASAKI and Yuichi SUGAI
3.8
ROLLING RESISTANCE STUDY OF GRAVELLY SAND MATERTAL ON LABORATORY SCALENuhindro Priagung \MDODO, Suseno KRAMADIBRATA, Abdul ROHMAN, Yudtr-idya WICAKSANA, Faj ar HERMAWAI.{
IV. ENVIRONMENTAL SCIENCE
4.1.
HIGH.EFFICIENT OF SO2 REMOVAL USING ACTTVATED CARBON FIBERMiftahul HUDA and Isao MOCHIDA
4,2.
GENERATION AND PREVENTION OF ACID DRAINAGES FROM MINE TAILINGS (REVrEw)Keiko SASAKI
tr-l8
TT.26
T1.32
ru-1
trI-10
III-17
III-28
III.36
III47
ru-55
III-64
ry-t
v1
rv-5
4.3.
4.4.
4.5.
4.6,
4.7.
4.8.
4.9.
4.10.
4.11.
4.t2.
4.13.
MDGD
ACID A}ID NON.ACID WASTE ROCKS ASSOCIATED WITH ACID MINE DRAINAGE GENERATION: A PRELIMINARY RESULT OF COLUMN TEST EXPEzuMENTCandra NUGRAHA, Hideki SHIIvIADA, Takashi SASAOKA, Masatomo ICHINOSE, Kikuo MATSUI, Evie H. TULAR, Imanuel MAIIEGE FTINDAMENTAL STUDY ON AMD.PREVENTION BY USING COMPACTED
WASTE ROCKS AT BE,[{AU COAL MINE, INDONESIA
Jiro OYA, Hideki SHIMADA, Takashi SASAOKA, Masatomo ICHINOSE, Kikuo MATSUI , Rianita PERTIWI and Andi M. FAJRIN FEASIBILITY STUDY FOR SUSTAINABLE AND ENVIRONMENT CONSCIOUS INFRASTRUCTURE DEVELOPMENT IN YOGYAKARTA, INDONESIA
Hideki SHIMADA, Hideaki NAKAGAWA, Takashi SASAOKA, and Kikuo MATSUI ASSESSMENT OF THE VOLCANIC DEBzuS FLOWS AND THE INLINDATION AREAS AT MERAPI VOLCANO AREA
Silmi FAUZIATI, Koichiro WATANABE IMMOBILIZATION OF MANGA].IESE FROM GROUNDWATERUSING LOW COST MATERI.ALS
Wahyu WILOPO, Keiko SASAKI, Tsuyoshi HIRAJIMA DEVELOPMENT OF CATALYST FOR TT{E REMOVAL OF PARTICULATE
MATTER FROM DIESEL EXI{AUSTS
Hajime KUSABA, I{ironobu SHIMOKAWA, Hisahiro EINAGA and Yasutake TERAOKA GLOBAL ENVIRONMENTAL IMPACTS OF CLIMATE CI{ANGE AND A REVIEW OF THE CHALLENGES IN IRAN
Hossein YOUSEFI, Sachio EHARA, Amin YOUSEFI PREPARATION OF HIGHLY ACTIVE AND
TIIERMALLY
STABLE SUPPORTED PEROVEKITE.TYPE OXIDE CATALYTS FOR PROPANE COMBUSTIONTeruaki Asada, Hajime Kusaba, Hisahiro Einaga, and Yasutake Teraoka IMPROVEMENT OF THE CATALYTIC PERFORMANCE OF La-K-Mn-O
PEROVSKITE OXIDES FOR DIESEL SOOT COMT]USTION
Hironobu SHIMOKAWA, Hajime
KUS$A,
Hisahiro EINAGA and Yasutake TERAOKA OXYGEN REDUCTION ELECTRODE USING CARBON-SUPPORTED LaMn I - yFeyO3 NANOPARTICLES PREPARED BY ITYDROLYSIS OFMETAL-EDTA t
COMPLEX
Lin Shao, Masayoshi Yuasa, Tatsuya Kida, Noboru Yamazoe, and Kengo Shimanoe DEVELOPMENT OF HIGH OXYGEN PERMEABLE MEMBRANE USING
ASYMMETRIC -STRUCTURE B ASED ON B ao.gslao.e5FeO3 -6 P EROV S KITE-TYPE OXIDE
K. WATANABE, Iv[. YUASA, T. KIDA, N. YAMAZOE, K. SIIIMANOE
TFIE CARBON DIOXIDE ADSORPT.TON EXPERIMENTS ON INDONESIA COAL SEAM, A CASE STUDY FROM KUT,{,I BASIN
Ferian ANGGARA, Hendra
AMIJAYA,
Lucas Donny SETIJADJI, DEENDARI,IANTO, BARLIN COz SEQUESTRATION, REUSE OF SOLID WASTE OF CARBIDE WELDINGPROCESS FOR MINERAL CARBONATION
Dewi K., Effendi A:J., and Syam D.A.
IV.12
IV-19
TV.25
rv,35
IV43
TV48
IV-50
rv-62
IV-64
TV-66
tv-68
rv-70
4.t4.
...,4.15.
vll
tv
-794.16, STUDY ON
TIIE
EFFECT OF MINERALS A}ID TTIEIR CHANGES IN ACID MINE DRAINAGE (AMD) FORMING IN COAL MINEGinting J. KUSUMA, Rudy S.
GAUIAMA,
and Maodor T. GULTOMV. POLICY AND NOVEL CARBON TECHNOLOGY
5.1.
5,2,
5.3.
5.4.
STUDY ON THE UTILIZATION OF FLYASH AS BACKFILLING MATEzuALS Takashi SASAOKA, Hideki SHIMADA and Kikuo MATSUI UPGRADING MECHANISM OF SOLID WASTE OF PALM OIL
MILL
USINGI{YDROTHERMAL TREATMENT.
Ahmad T. YULIANSYAH, Tsuyoshi HIRAJIMA, and Keiko SASAKI DEVELOPING A MODEL OF TAX AND PERMIT POLICIES FOR ABATEMENT THE COz EMISSION OF COAL
Rudianto
EKAWAN
PRELIMINARY STUDY OF LOW RANK COAL TO SECURE SUPPLY OFELECTRICTTY IN INDONESIA
Aryo P. WIBOWO and Fadhila A. ROSYID
6.1.
6.2.
6.3.
u.o.
.
6.5.
6.6.
VI. THERMAL ENERGY
APPLICATION OF CARBON FIBERS TO THERMAL ENGINEERING
Jun FUKAI and Koichi NAKASO RESEARCHES ON MPROVING THE PBRFORTvIANCE OF REFRIGERATION/AIR CONDITIONING SYSTEM IN OUR LABORATORY RELATED TO THE ENERGY SAVING/ENVIRONMENTAL PROTECTION TECNOLOGY
Ken KUWAHARA and Shigeru
KOYAMA
FIELD TESTS OF HORTZONTAL GROUND TIEAT EXCHANGERS USING COIL.LIKE TUBE
Hiroaki OKUBO, [Iikari FUJII, Ryuichi ITOI, Keita NISHI, Kunio
OI{YAMA
and Naokatsu CHOU
A
PRELIMINARY DESIGN ON ADSORPTION HEA.T PUMP USING ZEOLTTE FOR RECOVERING WASTE STEAMErfina OKTARI"ANI, Koichi NAKASO and Jun FUKAI THERMAL STRUCTURE OF AIRA CALDERA
Keiko FUJINO, Sachio EHARA and Toshiro
YAMANAKA
WATER INJECTION MONITORING INTIIE
GEOTHERMAL FIELD USINGMICROGRAVITY MEASUREMENT: A CASE STUDY OF KAMOJANG GEOTHERMAL FIELD, INDONESTA
Yayan SOFYAN, Yunus DAUD, Yustin
KAMAH
and Sachio EHARAIV-87
v-1
v-9
v-17
v-30
VI-1
VI-8
VI.1O
VI-17
vI-26
YT.29
VI-37
6,7,
ENERGY AND EXERGY ANALYSIS OF SINGLE FLASH GEOTHERMAL POWER PLANT, SABALAN, IRANSaeid JALILINASRABADY, Ryuichi ITOI, Hikari FUJII, Toshiaki TANAKA
6.8.
INTEGRATION AND ANALYSIS OF GEOPFTYSICS AND OIL WELLS DATA FOR STUDYING GEOTHERMAL ACTTVMIES ON GULF OF SUEZ, EGYPTMohamed Abdel
ZAHE&
Mohamed El NOUB Y, EssamGIIAMRY
and Sachio EHARAviii
YT47
6.9,
ITYDROTHERMAL MODEL OF UNGARAN VOLCA}IO, CENTRAL JAVA, INDONESIAAgus SETYAWAN
VII. PETROLEUM ENGINEERING
7.T.
A PRELIMINARY STUDY ON MICROBIAL ENHANCED OIL RECOVERY USING CO2 AS A NUTzuENT SOURCEIsty A. PURWASENA, Yuichi SUGAI and Kyuro SASAKI
7.2.
MICROBIAL ENHANCED OIL RECOVERY (MEOR): LABORATORY STUDY OF EXOGENOUS BACTERTAABILITY
TO ATTACK CRUDE OIL HYDROCARBON AND CHANGE CRUDE OIL PHYSICAL CHARACTERISTICSAmalia Yunita
HALM,
Dea lndiani ASTUTI, NuryatifUL!
SEPTORATNO SIREGAR7.3.
TI{E STABILITY ASSESMENT OF TIIE WELL PAD AND PIPELINE CORRIDOR IN THE GEOTHERMAL FIELDBudi
SULISTIJO, Adrian W KUSUMO and Wayan SENGARA7.4.
EVALUATION OF IN-SITU GAS CONTENT A}{D COALBED METHANE POTENTIAL IN QUANGNINH COALFIELD,VIETNAM
Phung Quoc H[JY, Kyuro SASAKI, Yuichi SUGAI, Tran Tu
BA
7,5,
BASIC STUDIES ON OIL-DEGRADING AND I{YDROGEN.PRODUCINGMICROORGANISMS FOR MICROBIAL CONVERSION OF CO2 INTO CH4 IN OIL RESERVOIR
Yuichi SUGAI, Toshiya
NIIMI,
Kyuro. SASAKI, Yoshiyuki HATTOzu, TsukasaMUKAIDANI,
Kazuhiro FUJIWARA and Komei OKATSUVIII. NEW MATERIALS RELATED TO CARBON RESOURCES
8.1.
CATHODE ACTIVE MATERI,ALS FOR POSTLIT}IruM-ION
BATTERYShigeto OKADA, Takayuki DOI and Jun-ichi
YAMAKI
8.2.
PREPARATION OF NANO-SIZED FUNCTIONAL MATERTALS USING LASER ABLATION IN LIQUIDSTakeshi TSUJI, Masataka NAKANISHI, Takeshi MIZUKI, Masaharu TSUJI, Takayrki DOI, Junichi
YAMAKI
8.3.
METAL NANOPARTICLES ON NANO.LEVEL-CONTROLLED CARBONSUPPORTS AS EFFICIENT CATALYSTS FOR HYDROGENATION OF AROMATIC COMPOUNDS
Mikihiro TAKASAKI, Kenji HIGASHI, Yukihiro
MOTOYAI{A,
Seong-HoYOON, Isao MOCHIDA and Hideo NAGASHIMA8.4.
ENERGY SAVING PROCESSES ACTIIEVED BY THE RU CATALYST BEARINGA
CARBON MONO-OXIDE LIGAND: LIEVELOMENT OF ENVIRONMENTALLY FzuENDLY POLYMER SYNTHESISNariaki HARADA, Hideo,NAGASHIMA, Yukihiro MOTOYAMA, Jyushiro YASUHARA
VI.54
vII-1
VII-9
VII-19
VII.26
VII-32
VIII.l VI[I.3
vm-5
VIII-7
lx
coz SEQUESTRATION, REUSE OF
SOLTDWASTE OF
CARBTDEWELDING PROCESS FOR MINERAL CARBONATION
Dewi K., Effendi A.J., and Syam D. A
Environmental Engineering, Faculty of Civil and Environmental Engineering, Institut Teknologi Bandung
ABSTRACT
Carbon dioxide (CO) is one of Green House Gases which is usually emittedfrom various industrtal processes to the ambient air without further treatment. There is no certain limitation
for
CO2 emission to the ambient air becausethis gas was considered to have no direct efect to human beings. Because there is no control
for
CO2 emission, CO2 concentration is continue to rise, causing the global warming phenomena. There ere severel techntques to control CO2, such as forestation, oquifer storage, injection to the ocean, and mineral carbonation. The first three methodsare subjected to control CO2for very big sources such as oil and gas exploration and coalJ'ired power plant. For a medium or small CO2 source the mineral carbonation which changes the COz gas to be the precipitate calcium carbonate (PCC) con be chosen. PCC has a good economical value since
it
can be used asfiller
in chemicalindustries (e.g. papea PVC, tires, pharmacy, and toothpaste industries). The COz removal has been performed tn a fritted midget tmpinger by passing the COz gas through the liquid gas absorber which was made
fro*
the solidwaste of carbide welding process. The source of CO2 was derivedfrom the COz refining facility in an oil company with concentration almost reach 90%. Various percentages of CO2 removal were achieved by varying the rate
of
CO2 gas and the moss of solid waste of carbide welding process. Very promising results were derived, and become the initial steps for further set up an appropriote design of a cheap and applicable CO2 removal reactor for a small
and medium source of CO2gas.
Keywords: Green house gases, precipitate calcium carbonate, fritted midget impinger, carbide welding process.
BACKGROUND
Carbon dioxide (CO, is considered to be the main Green House Gases (GHGs) since it constitutes about 50% of
GHGs in the atmosphere (See Figure 1). The main source of anthropogenic CO2 emissions during the past 20 years (about three quarters) is due to the combustion of fossil fuet. The rest is mainly due to land-use change, especially deforestation. Several industrial processes (such as oil refining and manufacturing of cement, lime, and steel) are significant sources of CO2. In global scale, the emission source of CO2 is described in Table
l.
Several techniques are available for carbon capture and storage (CCS) as written in Table 2. Among them, the mineral carbonation is a promising choice since it can utilize the waste material from industrial process and can be applied for a small to a medium scale of CO2 soul'ce. Many various types of solid alkaline waste materials are available in large amounts and are generally rich in calcium. Wastes that can be carbonated are iron and steel slag, municipal solid waste (MSW) incinerator ash, concrete wastes and several types of process ashes and dusts (Huijgen et al. 2004). The mineral carbonation is the concept of an accelerated carbonation process for storage of COz
b&
IV-79
.a
(Lackner 2OO2). One of the ways is just simply reacting COz with the alkaline substanc?, a.E. calcium or magnesium substance to produce the precipitate calcium carbonate (PCC).
Table 1. Emission Source of CO2
-
Global ScaleActivities
Fossil Fuel Usage Coal fired power plant Cement industry Oil and gas exploration Iron and steel Industry Chcmical industry Oit and gas refineries Other sources Biomass Usage Bioethanol dan bioenergy
Emission Number of
source
(MtonCOz/year)
4,942 1,175
638 269 470 N/A 90
303
10,539 932 798 646 379 50 33
9r
50% co?
r39icl!
51t r,t20 Total 7,88? 13,466
7'h o,
iarFlain 129,i cFC R.12
5%CFCR-il
Figure l. CO2 composition in the atmosphere
Source: IPCC Special Report on Carbon Dioxide Capture and Storage, 2000
In this research, the solid waste of carbide welding process is chosen as the source of alkaline substance in the form of slaked lime (Ca(OH)r). The slaked lime from the waste of carbide welding process originates from the reaction
of
calcium carbide and water, i.e. CaC2 + 2H2O
*
CzHz + Ca(OH)2. This slaked lime is then reacted with CO2 to produce the PCC by the reaction as follow: Ca(OH)z + COz --* CaCOr + HzO. PCC is used as filler in chemical industries, e.g. paper, paint, PVC, tires, Pharmacy, toothpaste, and etc. This research is a preliminary research to investigate the potential prospect of the carbonation process as alternative technology for CO2 abatement as well as the use of carbide welding process as the alternative materials f.:r the source of alkaline substanceMETHODOLOGY
Carbon dioxide with the purity more than 90% taken from the CO2 removal unit in oil and gas refinery was reacted with the solid waste of carbide welding process taken from a local small welding company (see Figure 2).
IV-80
CCS Component Capture
Transportation Geological storage
Table 2. Carbon Capture and Storage (CCS)
CCS Technology Post and Pre-combustion Oxyfuel combustion
lndustrial separation (natural gas processing, ammonia production)
Piping, shipping
Enhanced Oil Recovery GOR)
Gas or oil fields Saline formations
Enhanced Coal Bed Methane recovery (ECBM) Direct iqj ection (dissolution type)
Direct injection (lake type) Natural silicate mineral Waste material ocean storage
Mineral Cerbonation
The use of COz in industrial sector
Source
:
IPCC Special Report on Carbon Dioxide Capture and Storage, 2000(a)
(b)Figure 2.(a) Alkaline substance from the waste of carbide welding taken from a local smail welding company. (b) CO2 form CO2 removal unit using Methylethylamine (MEA) in oil and gas refinery
IV-8I
kontainer gas Jlotvnuter Auto Enission Analyzer trap gas asam
trap uap air
Jr i ued bub b le r i mpe nge r
Figure 3. Configuration of Simple continuous reactor
-
laboratory scaleTable 3. Laboratory analysis
Sample
Parameter Method Emission
Gas
Acid Gas
Trap Absorber
PrecipitateCO:
Conccntration pH Temperature Alkaliniry-Acidiry Calcium hardness Carbonate precipitate
NDIR
Electrometric Thermometer Acid Base Titration EDTATitration Gravimetric
l)
2) 2) 3)
2) 2) 2) 2)
3)
Note:
(l)
Before and during the reaction, (2) Before and afte.r the reaction, (3) After the reactionRESULT AND DISCUSSION
The comparison of results of chemical composition analysis of carbide welding waste is shown in Table 4. The local carbide welding waste has the smallest content of Ca(C)H)2 compared to others, i.e. aroun
d
5O%. This indicates that the slaked lime content in the solid waste of carbirie welding is site specific, therefore for new source of solidwaste the analytical composition should always be pe.rformred. Other substance in the carbide wekling solid waste was also identified which may influence the overall nrineral carbonation process.
IV-82 The absorbent for mineral carbonation was prepared by diluting certain amount of solid waste of carbide welding in the water. This absorbent was then filtered to derive the true diluted Ca(OH)z (denoted as filtered Ca(OH)2.).
Another form of absorbent was called unfiltered Ca(OH)2, which is made by simply diluted Ca(OH)2 without filtering process. The mineral carbonation took place in a simple continuous reactor in a laboratory scale depicted in Figure 3. The main reactor was the modified fritted bubbler impinger where CO2 was reacted with the filtered Ca(OH)2 or by the unfiltered Ca(OH)2 slurry to form PCC at the end of the reaction. The formed PCC was then measured by the gravimetric method and other physical and chemical parameters during mineral carbonations were also analyzed as shown in Thble 3.
Table 5 shows the reduction of Ca2* in the absorbent before and after mineral carbonation process in various flow
rates. The reduction of Ca2* related to the absorption of CO2 gas, therefore the reduction percentage also denotes the amount of COz which can be sequestrated. The existence reaction between Ca*2 and CO2 can also be identified by
the change of absorbent pH, as shown in Table 6. The absorbent pH decreases from around 12 before the reaction to around 6 to 7 after the reaction. The total amount of COz absorbed during mineral carbonation is shown in Figure
4. This figure also illustrates the influence of flow rates and absorbent characteristics to the amount of absorbed CO2.
The higher amount of filtered Ca(OH)2 results in a higher amount of COz absorbed, while the unfiltered of Ca(OH)2 can inhibit the absorption process. Solid in the form of Ca(OH)z slurry may increase the gas
Thble 4. Chemical Composition of Carbide welding waste (% weight, wet basis)
Parameter Source
International Industrial
Gas
Local Carbide WeldingUSAPatent
5997833 Ltd.
WasteCa(OH)z CaCOr Me(oFI),
sio2 Al: O:
Fe: Or NarO PzOs
Other minerals Carbon (u coke)
Water vapor
Ca2*
Stait 130.08
r33.75 t39.24 140.87
80.5
3.4 1.9
0.2 0.7 0.7
I 3.6
8
92.s 1.8
1.5
1.6
50.280
0.236 2.4r5 0.489 0.r57 0.007
<0.01
1s.646 32.908
Thble 5. Ca2* Concentration in the absorbent used in mineral carbonation rng/ 100 mL Ca2*
l,292Lpm
Mass of Carbide Welding Waste (mg/100 ml)
2;10 5.40 8.r0 10.80
Ca2*
End 36.03
39.09 3 l.rs
26.26
94.05 94.66 108. l0
I t4.61
72.30 70.78 77.63 81.36
ACa2* %
Ca2*
Start
0,496 Lpm Ca2*
End
ACa* o/o
48.68 64.86 138.63
140.77
71.r5 49.47
67,48 91.30
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Thbte 6. The change of absorbent pH during mineral carbonation
Mass of Carbide Welding Waste pH ofAbsorbent Flow-rate (Lpm)
(mg/100 mL) Start End
0,496 0 6.68 4.48
8.1 t2.9 6.6
10.8 t2.63 6.71
1,292 0 6.78 5.48
2.7 12.26 7.39
5.4 t2.24 7.22
8.1 r2.88 6.9s
10.8 12.63 7.04
Figure
4.
Influence of Absorbent Characteristics and Gas Flowrate on Absorbed CO2holdup and the area contact befween gas-liquid and also prevent the combine of air bubbles. A higher flowrate (1.292 Lpm compared to 0.496 Lpm) make more CO2 absorbed during the reaction.
For the future improvement of the research, another reactor shall be set up in order to be able to measure the real time measurement of pH and COz concentration during the reaction (see Figure 5).
s.rirq E tarpa erirg
rq,.@
3r00.m
26m.q)
2rm.00
t6m.0
il00.m
ffi
ffi
0,496 Lpm 1,292 Lpm
E
o
2.70 5,{0 8,10 10,80 1.7 5,1 E. t0 10.80 nnsse lirnbrh hr kerbld (3) / 100 rnl rir distilari
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CO2, N2 Car
furly
Figure 5. Future set up of batch reactor for mineral carbonation
CONGLUSION
Carbonation of calcium-rich materials is an interesting option for simultaneously reducing CO2 emissions and utilizes industrial waste. The use of natural calcium for mineral carbonation would require a large-scale operation.
On the other hand, industrial waste such as solid waste from carbide welding process could provide a low-cost
source of calcium rich materials. If the produced calcium carbonate could reach the purity specifications of PCC, solid waste of carbide welding could be used to produce valuable product, while also reducing CO2 emissions and preserving natural mineral resources. Although the global CO2 storage potential by carbonating solid waste of
carbide welding is small in comparison with other CO2 storage options, it can reduce the annual CO2 emissions for an individual industrial plant.
In this preliminary research,
it
can be concluded that mineral carbonation is a very promising process for CO2abatement for a smatl scale source. The solid waste from carbide welding process has enough amount of Ca(OH)2 which can be used as the source of alkaline substance. However, since the amount of Ca(OH)2 in the solid waste of
carbide welding is various or site specific, the analysis of Ca(OH)2 for a new source of solid waste of carbide welding should always be performed. The carbonation process has already been done in a simple continuous reactor, which mainly consist of a modified friued bubbler impinger. The absorbent in the form of filtered Ca(OH)z gives beffer absorption capacity than unfiltered one in absorbing the CO2, and a higher reactor flowrate also gives a better absorption performance.
Another reactor set up
with
more complete and thorough la.boratory analysis for mineral carbonation using the solid waste of carbide welding shall be carried out in the future work to improve the performance of carbonation process.v/
(oH)z
2t
t
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REFERENCES
IPCC, Special Report on Carbon Dioxide Capture and Storage, (2000).
Halmann M.M and Steinberg M., Greenhouse Gas Carbon Dioxide Mitigation
-
Science and Technology. Florida, U.S.: Lewis publishers. (1999).Huigen, W.J.J et al, Mineral CO2 Sequestration in Alkaline Solid Residues Q004).
Lackner K.S. Carbonate Chemistry
for
Sequestering Fossi/ Carbon. Annu. Rev.Energy Environ., 21, pp.l93-232.(2002).
Sebastian Teir,, Reduction of CO2 Emission by Producing Calcium Carbons from Calcium Silicates and Steel
Maktng Slag, (2006).
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