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TRANSCRIPT
Korean Chem. Eng. Res., Vol. 42, No. 1, February, 2004, pp. 1-9
·
305-343 71-2(2004 1 20 , 2004 1 31 )
Hydrogen & Fuel Cell Technology
Jae-Ek Son
Korea Institute of Energy Research,71-2, Jang-dong, Yuseong-gu, Daejeon 305-343, Korea(Received 20 January 2004; accepted 31 January 2004)
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PEMFC8 DMFC Z yz$ @| %- h:~.
Abstract − Among various technologies using hydrogen-energy, fuel cells have been considered as the most energy efficient
technology. A conventional combustion-based power plant typically generates electricity at efficiencies of 33 to 35 percent,
while fuel cell plants can generate electricity at efficiencies of up to 60 percent. When fuel cells are used to generate electricity
and heat (co-generation), they can reach efficiencies of up to 85 percent. Moreover, fuel cells generate virtually zero pollution
including greenhouse gases such as CO2. Therefore, the fuel cells are believed as a most promising alternative power produc-
ing technology, which can solve global problems facing 21st century such as exhaustion of fossil fuels and environmental pol-lution at the same time. In this review, recent trends in fuel cell R&D are summarized focusing on PEMFC and DMFC which
are closest to the practical use and can be used for batteries, electrical power sources for automobiles and immobile structures
such as buildings.
Key words: Hydrogen Energy, Fuel Cell, Proton Exchange Membrane Fuel Cell (PEMFC), Direct Methanol Fuel Cell (DMFC)
1.
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†To whom correspondence should be addressed.E-mail: [email protected]
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[19]. Lurgi Gmbh F~Eo SEh ^)) $
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Table 2. Feedstocks for hydrogen [34]
CO2/H2 Technology
0.25 Steam methane reforming0.31 Steam pentane reforming0.33 Partial oxidation of methane0.59 Partial oxidation of heavy oil1.0 Partial oxidation of coal
Table 1. Feedstocks for hydrogen [34]
Source World capacity (1988), %
Natural gas 48Petroleum 30
Coal 18Electrolysis 4
Korean Chem. Eng. Res., Vol. 42, No. 1, February, 2004
4
e
c1h + " å8 I À¿ 4Nw a,.
4Ô6 ÊÔ 2) c «, FS 260-370oC cK
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K = D7 $ ED» ) ÛA,.
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H2+1/2 O2hH2O+58.6 kcal/mol (unwanted)
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Ø°A,. ! D< ") Pt/alumina(100-160oC)[46], Ru/
alumina(100-180oC)[47], Au/Fe2O3(60-80oC)[48] ÁK $
! ÔW 100-200oC, à~ 4 "à I GOW 7 5,000-30,000 hr−1
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3.
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diffusion layer), ¬ô(separater) Á) 8K, ];"#) F,
F, ¬ô ¡g _"# Á a,.
23F7 8 zm F 23 G" c1o 9r ++
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) b F¸h wêg I » <,. x F F S
ÓD F I| c1 m 9r7 e4 Ô < FWW
D x°9 <,. PEMFC LM Ä" phenol sulfonic Ü m
polystyrene sulfonic Ü Á !IJ y l` z
¡7 ÆIJ,. - PEMFC "# 1970 | LM
¼ perfluorosulfonic acid Ü(Nafion) !I`z &<
y Ns â ae,[49]. ·7 ! Ô F Ü/
y¬ b` °(o Ç,[50].
Ô Teflon6 < 8), ~ #c(SO3H)"h D74
a,. #c" ýW D) , 1h "G) I Ü/
E b, Ý Ô FWWh Â,. Ô FWW
Ô Ü D' á ' y a,4 J a,
CF2h 4S "G8) !)` âA è6,. Dow
Chemical Ashai Chemical Á Ô6 < 8 b
, side chain D7K, #c" ýWD Ô b, Ý
perfluorosulfonic acid Ü I|, b, Ns¼ b4 IJ,
[51]. W.L. Gore ¥[ ø 77Ó) !< Nafion Ü
LMI|, "$ ÖW Ns6 "Ó R6Wh ; aeK,
V$) D' Ý F-F ðÓ(MEA)h *
cI4 a,[52-53]. F Ü 9 ÊD Ü LM, ÊDt
/Dt Ü -¬4 4Ô! Ü LM %U) I4 aK, 284
a ªÌ ) polyethersulfone(PSU), poly ether ether keton
Table 3. Main characteristics of each reforming process
Technology Main Reaction Characteristics Conc. of H2(%) Company
STR CH4+H2O=CO+3H2, H=+49.7 kcal/mol
· Slow endothermic · Indirect heating· Larger reactor volume· Slow response time· High efficiency
65-75 Plug power [40]
POX CH4+1/2O2CO+2H2 H=−9 kcal/mol
· Fast exothermic· Direct heating· Fast start-up and response· Low efficiency
30-40 Nuvera [41]
ATR Balance of STR & POX · Combination of STR & POX· Direct heating· Fast start-up and response
40-50 Johnson matthey [42]
Table 4. Characteristics of polymer electrolyte membranes
MembranePower density
(kW/m2)Life time
(*1,000 hr)
1959-19611962-19651966-19671968-19701971-1980
Phenol sulfonicPolystyrene sulfonicPolytriflurostyrene sulfonicNafion experimentalNafion procudtion
0.05-0.10.4-0.60.75-0.8
0.8-16-8
0.3-10.3-2
0.75-0.80.8-1
10-2000
42 1 2004 2
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Á U$,[54-56].
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q= , =½ m =½ ½ D' «< F") Ð
NL a,. F s 6Fà(overpotential) 236 G"
á nh b, 23 7 20 mV7, G" 7
400 mV ê 6Fà ÂK, 6Fà OCV(open
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E ëì <, - r Ö< O-O è
6 y< Pt-O m Pt-OH , 4L FS Y|I
, 6c1 * D Á a,. E c1
2L FS Y|I ) S u < \
B6y W èy) ÐNL a,[50].
23 " è9 : LD¡h ! « 23
| a CO < F ÊI :o, G" "
6Fà Ø] FÓ 23F7 ÙÚ Ns^,9 <,. >
? G" 6Fà Ø]N W 28) =½ F½ Á
!I| =½ rS O ¬ d-band vacancy I|
á Ù6h b4 a,[57-59]. m< >? =½ !< 23 23
) L D¡h ! « M*I Q(CO, CO2 Á) <
8 7È " LM F ! ¨© < 28 AF
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H2 2Pth 2H/Pt
H/Pth Pt H+ e−
CO/PtOHadsh Pt CO2 H+ e−
C ñÈ Pt-CO è Pt-H b, ÖI" õ:K, CO 10 ppm
ýW n ;+< ÊIh b,. h C< èÀ)
=½6 ,< ½ ½ "h F") !<,. ·7 b
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« hot spot) " è, 4S Ü ¾1, "
v Á :D M*<,. .< : èI" C F E
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WBI j z, U$) 28 Ô ½) Cr,
Ni, Co, Fe[72-74] Á a,.
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! Á + !9 $< y ¨b Á,.
46 ÊD& MEA LM C< 28), Los Alamos National
Laboratory u½ =½ 77Ó) U`$ carbon
black ! )` =½ " " 7 1/10) ; G
IJK[75], ) 23 « 7 0.05 mg/cm2 )W
"b, ë «< Â MEA _ D ,[76].
m ,É MEA Ns À¿) FE =6h ; À¿
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Fà Ø]K, å~ÿWh D^,. .< À¿) W. L. Gore
« FE =6h 7 10 micron) _I|, « «<
Â4 a,[52, 53].
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F¿(separate electrode method) "h ,G F"FW D
7 §6 î Á 4y^ 6y Þ j
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permeability
GORE-SELECT 1,100 20 0.52a, 0.53b 26 32 3.7GORE-SELECT 1,100 5 0.28a 56 - -GORE-SELECT 900 12 0.96b 80 43 12.9Nafion 117 1,100 200 0.14a, 0.10b 5-7 34 1.0 20%Nafion 112 1,100 60 0.10b 17 34 3.3Dow 800 100 0.15b 15 56 4.0az-direction, sulfuric acid immersed sample measured with a four-point probe.bx-y direction, high-frequency measurement for membrane immersed in deionized water.cExpressed as percent of membrane dry weight.dHydraulic permeability relative to Nafion 117.
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