Teknologi Hidrogen Dan Fuel Cell ENGLISH
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Transcript of Teknologi Hidrogen Dan Fuel Cell ENGLISH
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Teknologi H
GROUP H :
1. Suci Ardiana R I 051200
2. To!i "i#anarko $. I 05120%
%. S&a'ra (au!il I 051%)))
*. Ina I 051*)))
5. Ta+!iul I 051*)))
Hydrogen production by steam reforming of ligas (LNG) over mesoporous Ni/Al2! catalyst
"#$A%assisted impregnation met&o
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1.In,roduc,ion
I,-+ ell/knon ,&a, &drogen can +ere a+ a rene
energ carrier due ,o i,-+ non/3ollu,ing na,ure.Hdrogen can e 3roduc,ed :
4uel/3roce++ing o4 &drocaron+
alco&ol and
6io/deried co!3ound+
O,&er earl/+,age &drogen 3roduc,ion ,ec&nologie
$lec,rol+i+ and
P&o,o/ca,al,ic a,er +3li,,ing
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In indu+,r +cale !e,&ane +,ea! re4or!ing i+ u+ed 4or la&drogen 3roduc,ion ecau+e i,-+ !ore a7ordale.
In ,&i+ 3roce++ nickel/ca,al+, i+ u+ed i,-+ 8i2Al2O% !e
i,& $9TA/a++i+,ed i!3regna,ion !e,&od &ic& 4unc,ion i+!e,al di+3er+ion.
$9TA/a++i,ed i!3regna,ion !e,&od i+ e)3ec,ed ,o e eci
1. !e,al/+u33or, in,erac,ion e,een nickel +3ecie+ and+u33or,
2. nickel di+3er+ion
%. ;e,&ane ad+or3,ion ca3aci, o4 8i2AlO% ca,al+, co!,&e conen,ional i!3regna,ion !e,&od.
Seeral c&arac,eri
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A !e+o3orou+ alu!ina +u33or, a+ 3re3ared an e3o)ide
+ol>gel !e,&od according ,o ,&e +i!ilar !e,&od+ re3or,ed in3reiou+ +,udie+
a. 11.* g o4 alu!inu! 3recur+or ?alu!inu! ni,ra,e nona&di++oled in 0 !l o4 an&drou+ e,&anol i,& igorou+ +,4or +ucien, &dra,ion o4 !e,al +3ecie+ 1. !l o4 di+,i
a+ ,&en added ,o ,&e +olu,ion.. 21.* !l o4 3ro3lene o)ide &ic& ac,ed a+ a gela,ion a
in,roduced in,o ,&e +olu,ion ,o genera,e &dro)l grou3++3ecie+ and ,o induce conden+a,ion reac,ion e,e+3ecie+.
c. A4,er +,irring ,&e +olu,ion 4or +eeral !inu,e+ a &i,e
o,ained. T&e gel a+ aged 4or 2 da+ and ,&en i, a+ d
2.1. Pre3ara,ion o4 !e+o3orou+ alu!ina +u33ore3o)ide/drien +ol>gel !e,&od
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2.2. Preparation of nickel catalyst supported on mesoporous
alumina support by an EDTA-assisted impregnation method
8ickel 3recur+o3re3ared :
1. di++oling 3recur+or in a,er ?Solu,
2. 2.0 g o4 $9TA
!l o4 di+,ill?Solu,ion 6@.
%. Solu,ion 6 a!!onia +olu,
*. Solu,ion A a++olu,ion C ?S
5. 1.0 g o4 !+u33or, ?;A@ !l o4 di+,illed
. 8i,ric acid dro3i+e in,o?;i),ure F@.
B. Solu,ion 9 ;i),ure F ?4onickel +3ecie+
?;i),ure G@.. T&e ;i),ure G
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2.%. 9e,er!ina,ion o4 3H
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2.4.Characterizations
1. Nitrogen Analisis Adsorpsi-Desorpsi Di 77 K Menggunakan B!"#$% Mini && 'B! (epa
$)a!ine ,e),ural 3ro3er,ie+ o4 +u33or, ?;A@ and ca,al+,+ ?8i$;A and Ni*MA)+,+
2. &C%s-1& '"hi/adzu)
To e)a!ine 8i loading o4 ,&e ca,al+,+. $ac& ca,al+, a+ 3re,rea,ed i,& a !i),ure o&droc&loric acid ?1:% olu!e ra,io@. T&e !e,al +olu,ion a+ ,&en !i)ed i,& deioni
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2.. Ca,a
Ca,al,ic 3er4or!ance in ,er!+ o4 J8G coner+ion
&drogen ield a+ calcula,ed according ,o ,&e 4oeua,ion+.
J8G coner+ion?K@ L ? 1 M @ ) 100
Hdrogen ield?K@ L ) 100
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0. $";!6" AND D&"C;"
0.2. 6e,tural %roperties
I, a+ o+ered ,&a, 8i$;A and 8i;A ca,al+,+ +&oed +!
ni,rogen ad+or3,ion ,&an ;A +u33or,. T&i+ indica,e+ ,!e+o3orou+ +,ruc,ure o4 ;A +u33or, a+ +igni'can,l locked +3ecie+ during ,&e i!3regna,ion +,e3 4or 8i$;A ca,al+, and dui!3regna,ion +,e3 4or 8i;A ca,al+,.
8i$;A ca,al+, +&oed larger ni,rogen ad+or3,ion ,&aca,al+,. T&i+ i+ ecau+e nickel +3ecie+ o4 8i$;A ca,al+, eaggrega,ed on 3o+i,iel/c&arged ;A +u33or, ia $9TAi!3regna,ion co!3ared ,o ,&o+e o4 8i;A ca,al+,.
0.1 D6A-assisted i/pregnation /ethod
U+ed 4or ,&e 3re3ara,ion o4 8i$;A ca,al+,
L
L Q $9TA
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0.0. Crstalline structure and reduction
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3.5. Methane adsorption of reduced catalysts
CH4TPD analyses were conducted to measure methane adsorptionreduced NiE/MA and Ni/MA catalysts The amount of adsor!ed CH4 oncatalysts was calculated from the CH4TPD profiles "t was re#ealed thaNiE/MA catalyst e$hi!ited lar%er amount of adsor!ed CH4 than the re
catalyst This is !ecause the reduced NiE/MA catalyst retained lar%er amohydro%en&!indin% sites than the reduced Ni/MA catalyst
3.6. Hydrogen production by steam reforming of LNG
'N( con#ersion and hydro%en yield o#er !oth NiE/MA and Ni/MA csta!le durin% the )* h&reaction+ implyin% that deacti#ation !eha#iors s
sinterin% and car!on deposition were effecti#ely pre#ented o#er the catalyAdditional catalytic tests were conducted under the same 'N( con
-.01 o#er NiE/MA and Ni/MA catalysts !y chan%in% contact time for !otis interestin% to note that H2/C3 molar ratio and C32/C3 molar ratio catalyst were smaller than those o#er Ni/MA catalyst -Ta!le *1 under thcon#ersion le#el Considerin% hi%h hydro%en yield of NiE/MA catalyst Ni/MA catalyst+ it can !e inferred NiE/MA catalyst was relati#ely effecti#e
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Gambar ' 2 LNG onversion dan Hydrogen yield atalis Ni"/*
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a. A !e+o3orou+ 8iAl2O% ca,al+, a+ 3re3ared an $9i!3regna,ion !e,&od ?8i$;A@ and i, a+ a33lied ,o ,&3roduc,ion +,ea! re4or!ing o4 J8G.
. A !e+o3orou+ 8iAl2O% ca,al+, a+ al+o 3re3ared a ci!3regna,ion !e,&od ?8i;A@ 4or co!3ari+on 3ur3o+e. $i!3regna,ion a33lied 4or ,&e 3re3ara,ion o4 8i$;A cac&ieed ia ,&e Coulo!ic in,erac,ion e,een 3o+i,i&dro)l grou3+ ? OH2@ on ;A +u33or, and 8i?$9TA@anion+. A+ a re+ul, ,e),ural 3ro3er,ie+ and !e,al>+u33or, i8i$;A ca,al+, ere en&anced co!3ared ,o ,&o+e o4 8i;A
c. T&e reduced 8i$;A ca,al+, re,ained +!aller nickel 3+&oed &ig&er nickel di+3er+ion ,&an ,&e reduced 8i;A ca
d. Fur,&er!ore ,&e a!oun, o4 ad+ored CH* oer ,&e reduca,al+, a+ larger ,&an ,&a, oer ,&e reduced 8i;A ca,
+,ea! re4or!ing o4 J8G con+euen,l 8i$;A ca,al+,!e,&ane ad+or3,ion ca3aci, e)&ii,ed e,,er ca,al,ic
. Conclusions
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THA8 (OUT$RI;A ASIH