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Tiêu đề Phân Tích Electron Trong Hóa Phân Tích Phần 8
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XPS spectra of commercial Ruhrc.hemie cazaly~ in Si 2p region... XPS spectra of commerded Ru]u'chemie catalys~ in O Is region... XPS spectra of comznerdal I~u]~chem~e catalyst in Cu 2p r

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FiEm-e 12 Y~S spectTa of commercial ] ~ r c h e m i e ~talyst in Fe 21) region (~) fol]o~-mg ca]dnat]on

of (a) to 112 at 300 °C

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~ l e llescrip~imc

Figure 13 XPS spectra of commercial Ruhrc.hemie cazaly~ in Si 2p region (a) foDowing calch~tion

for 16 ba-s at 300 =C; (b) following exposure of (a) to CO at 300 °C; (c) f o n o w i ~ exposure

of (a) to }t_- at 300 °C

67

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'Fi~.u'e I4 XPS spectra of" con'~n~da.1 R",z~daemie cat ~lyst in If 2p ant1 C ls ~regions (a} following

c ~ c ~ a t i o n fo~ 16 h~s at 300 °C; (b) follo~i~g e~os~Jre of (a) to CO at $00 • C; (c)fo]]owh~g e.~os'=e of (a) to ~ at 300 °C

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Fi~uTe 15 XPS spectra of commerded Ru]u'chemie catalys~ in O Is region (a) following calcination

for 16 hrs a~ 300 ~C; (b) foUo~ring ~posare of (a) to CO at 300 °C; (c) followiag ~ o s ~ r e

of (a) to ~I= at 300 °C

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Lsmiple De,,~,,t'~tion: ~

TE~S/~( I ] ~ S I T Y

Figure 16 XPS spectra of comznerdal I~u]~chem~e catalyst in Cu 2p region (a) foUowing calcination

for 16 ]~s at 300 oC; (b) fol]o~;~g exposure of (a) to CO at 300 oC; (c) following exposure

of (a) to H2 a~ 300 °C

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Time (rain)

Figure 17 Isothermal reduction p r o ~ e in ~I~ for calcined {16 hrs in O~ at 300 °C) ~rnp|e of 2,5 wt

% Fe/Si02

71

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Temperature (Oc)

Figure 18 T P R profile in H2 at 20 °C/miu for saznple of 25 wt % Fe/Si02 that had been pre~ously

txeazed for 15 bxs in H2 at 300 "C

?2

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%

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Figx~e 19 XP5 spectra of 25 "~1% Fe/SiO2 in Fe 21) region following calci~adon fox 16 h~s a~ 300

°C and subsequent txeatment in H2 for 16 ]~'s at 300 °C

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2 5 0 0 2 0 0 0 1800 1 6 0 0

Wavenumber (cm " 1 )

1300

16 ]lrs at 300 °C and subsequently z~-eatect in ]~z for 16 ]n~ at 300 °C ~rh~ uppermost

spectrum was o b t a i u ~ followiug exposure of the sa~np]e to 10 tort of ~qO for 15 rain,

foUowed by e~cuation T/~e second spectrum was obtained immediately a~te~ admission

in the ¢ontinuiug presence of gaseous Oz

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Figure 21 FT-IR spec~m o f NO a ~ o r b e d at 25 °C on 25 ~ % Fe/SiOz containing 1 ~ t % K that

had been calcined for 16 ]~'s s t 300 °C and subsequently treated in H2 for 16 hrs at 300

°C The uppermost spectrum was obt.zined following exposure of the sample t o 10 ~ r of

NO for 15 m ~ followed by e ~ c u a ~ o n T h e second spectrum was obtalned immediately

15 mJn intervals in the continuing presence o f gaseous 02

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