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1.
EFFECT OF CATALYST PRETREATMENT ON THE OXIDATION OF CARBON MONOXIDE OVER Au/NiO CATALYST 总被引:4,自引:0,他引:4
《中国化学快报》1995,(4)
EFFECTOFCATALYSTPRETREATMENTONTHEOXIDATIONOFCARBONMONOXIDEOVERAu/NiOCATALYSTEFFECTOFCATALYSTPRETREATMENTONTHEOXIDATIONOFCARBO... 相似文献
2.
《天然气化学杂志》1994,(4)
The effects of Y_2O_3 on the property of NiO/Al_2O_3 catalyst forcatalytic partial oxidation of methane were investigated in a continuous flowfixed bed reactor(20 mm i.d.,860 mm long).The catalysts werecharacterized by XRD and pore measurement.For comparison,similar studieswere carried out for the catalysts loaded with Zr or W oxide.The results showthat different additives and impregnating methods could greatly affect thedispersion of component Ni.The catalytic activity,the selectivity to CO andthe stability are improved because of the less facile interation between thesupport and nickel oxide,greater surface area and better dispersion of metalNi for NiO/Al_2O_3 catalyst modified by Y_2O_3. 相似文献
3.
EFFECTS OF ALKALI AND RARE EATTH METAL OXIDES ON THE THERMAL STABILITY AND THE CARBON DEPOSITION OVER A NiO/Al_2O_3 CATALYST 下载免费PDF全文
LIU Sheng-Lin MIAO Qing XIONG Guo-Xing * SHENG Shi-Shan CHEN Hen-Rong State Key Laboratory of Catalysis Dalian Institute of Chemical Physics The Chinese Academy of Sciences Dalian Liaoning HKmm〗 《天然气化学杂志》1998,7(3):189-197
采用固定床流动反应装置、CO吸附、TG、TPO、XPS和XRD等手段考察了NiO/Al2O3和LiNiLaO/Al2O3催化剂上的甲烷部分氧化反应。实验结果表明,LiNiLaO/Al2O3对甲烷部分氧化反应具有较高的反应活性。锂和镧的添加不仅改善了活性组分镍的分散度,而且提高了NiO/Al2O3的抗积碳能力和热稳定性 相似文献
4.
《中国化学快报》1991,(11)
In this paper, instead of with the more expensive Fourier Transform Infrared Spectrometer(FTIR) a new technique of Temperature Programmed Transient Response(TP-TR) has been used with gas chromatography. Therefore, the TP-TR will be applied more widespreadly than ever before. With the technique of TP-TR and electric conductivity, the study is on the reaction mechanism and the adsorption behavior of the reactants and products to the present catalyst Mo-V-Nb/Al_2O_3 in the reaction from ethane through oxydehydrogenation to ethylene as the product. By Range-Kutta-Gill and Margarat methods, the kinetic parameters of the reaction elementary steps (i.e. rate constants, active energies and frequency factors) have been evaluated. The mathematical treatment coincides with the experimental results. 相似文献
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《天然气化学杂志》1994,(1)
A series of highly dispersed bismuth molybdate series catulyst,Bi_xpMo_(12)O_y(x=1~8,y=40~61),were prepared from12-molybdophospho-ric acid under acidic condition.By means of IR and XRD,we found that thebasic composition of the catalysts wasα-Bi_2Mo_3O_(12)/MoO_,and the activity foroxidationof propane was ascribed to the co-effect ofα-Bi_2Mo_3O_(12)andMoO_3 probably. 相似文献
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lntroductionTheconversi0nofnaturalgast0syngasviQtheCatalyticPartialOxidaion(CPO)ofCH4(Eq.l)lledlethibitsthepotentiaIt0replaceconventionalsteamreforming(Eq.2),withasubstalialreductioninplantsizc.Thisproccssisnotcncrg}intensivc.andalso}'ieldss}.nthesisgasx`.ithH2/COmolarratioof2.O.x`hichissuitabIcforman}'chcmicalproccsscs-suchasthcproductionofmethanoIovcrCu/Zn0catal}'st(Eq.3)andFischcr-Tropschs}nthcsisovcrCo'CucataI}'sts(Eq.4).CO 2H2-CH30H(3)nCO 2nH2-C,,H(2,, l) nH2O(4)Atprcscnt-… 相似文献
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PARTIALOXIDATIONOFMETHANEOVERNiO/Al2O3MODIFIEDBYMETALOXIDES*MiaoQing,XiongGuoxing**,XuLing,ShengShishan,GuoXiexian(StateKeyLa... 相似文献
8.
IntroductionOxidativccouplingofmethanc(0CM)hasbccnthcsubjcctofmuchintcrcstrcccntl}Man}'mctaloxides,alkali-mctaI-promotcdmctaloxidcs-mixcdmcta1oxidcsandchlorinc-prom0tedmCtuloxidcshavcbecnf0undtobcactivcfor0CMHot` cvcr.thcrcisatprcscntnoclearagreemcntaboutthcmcchanismofthecouplingrcaction.T\`omodclsll1.thcthdeal-rcdoxandthcLangmuir-Hinshtt-oodmcchanisms.havcbccndcvcIopcdtodcscr1bc0CMreation-thecsscntialdiffercnccbctt"ccnthctt"omodclsisthatthclattcrinvolvcsadsorbedmothancasarcactionintcrmcd… 相似文献
9.
It is showed that La_2O_3 and NiO could disperse on γ-Al_2O_3 as a monolayer and theirutmost monolayer capacities determined by quantitative XRD are 0.28g/100m~2 and 0.09g/100m~2respectively. In the methanation catalyst, Ni/La_2O_3/γ-Al_2O_3, the La_2O_3 is dispersed on thesurface of γ-Al_2O_3 as a monolayer and the metallic nickel crystallites are supported on thesurface with La_2O_3. It has been found by the XRD peak broadening that the average size ofnickel crystallites on the surface with La_2O_3 is much smaller than that without La_2O_3. Thismay be one of the main reasons for the increase of activity and thermostability of the La_2O_3containing methanation catalyst. This idea of modifying support surface by monolayercompound can also be applied to other catalysts. 相似文献
10.
XU Long-Ya WANG Qing-Xia XU Yi-De YANG Li HUANG Jia-Sheng Dalian Institute of Chemical Physics Academia SinicaDalian. Liaoning State Key Laboratory of CatalysisDalian Institute of Chemical Physics Academia SinicaDalian LJaoning 《天然气化学杂志》1995,(4)
K_2O and MnO are two kinds of necessary promoters to theselective production of light alkenes from CO hydrogenation over silicalite-2(Si-2) zeolite supported Fe catalyst. The addition of both K_2O and MnOpromoters into Fe/Si-2 catalyst leads to a remarkable increase in the COconversion and the selectivity to light oletins. Silicalite-2 zeolite as Fe-MnOcatalyst support can suppress the formation of α-Fe_2MnO_3 or/andα-Fe_(2-y)Mn_yO_3 as Well as α-Fe_2O_3 and/or α-Mn_2O_3, being favorable for(?)ncreasing the dispersion of active metal component. So MnO can promotethe reduction of Fe~(3-) and enhance the capacity of CO adsorption, which canimprove the activity of the activity of the catalyst for CO hydrogenation. While K_2Opromoter is unfavorable for reduction of Fe~(3-) to some degree with formation of Fe~(2-) as a new species after reduction. However, K_2O promoter can enhance the capacity and strength of CO adsorption greatly.So K_2O can alsoimprove the activity of catalyst for CO hydrogenation. 相似文献
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13.
《天然气化学杂志》1994,(2)
The modification effects of TiO_2 towards Cu or CuO in supportedCuO-ZnO/Al_2O_3-TiO_2 catalyst were studied by XPS,TPD and test reaction.XPS showed that TiO_2 additive improved the dispersity of CuO or Cu in cata-lyst.TPR showed that the reduction temperature(Tr)of CuO in CuO-ZnO/Al_2O_3-TiO_2 increased with the content of TiO_2.XPS showed that the Eb valueof Cu in TiO_2 containing catalyst(Eb=993.7 eV) was larger than that inTiO_2 free catalyst(Eb=932.9 eV).These indicate that TiO_2 displayed elec-tronic effect on catalyst.Both structural effect improving the dispersity of Cuand electronic effect weakening the bond strength of Cu-S in catalyst caused theS-resistance of CuO-ZnO /Al_2O_3-TiO_2 catalyst greatly improved. 相似文献
14.
WU Jin-Gang LI Shu-BenState Key laboratory of Oxo Synthesis Selective Oxidation Ijmzhau Institute of Chemical Physics Academa Smica Lanzhou Gansu 《天然气化学杂志》1995,(1)
EPR and Raman spectroscopy have been used to characterize the catalyst. F-centers with EPR parameter of g=2. 0046 form when gas phase oxygen is admitted onto the catalyst reduced with methane at 800℃- Molecular oxygen plays an induced role in the electron transfer from W4 to the oxygen ion vacancy which is produced by methane reduction. Raman spectra give the further evidence for the production of lattice oxygen from molecular oxygen. 相似文献
15.
XU Long-Ya WANG Qing-Xia XU Yi-De HUANG Jia-ShengDalian Institute of Chemical Physics Academia SinicaDalian Liaoning State Key Laboratory of CatalysisDalian Institute of Chemical Physics. Academia SinicaDalian Liaoning To whom correspondence should be addressed. 《天然气化学杂志》1995,(3)
The activity and the selectivity to light alkenes of silicalite-2 (Si-2) zeolite supported F'e catalyst tor CO hydrogenation can he improved obviously with the addition of K2O and MnO promoters. The results of CO hydrogenation, CO-TPD, CO/H2-TPSR, C2H4/H2-TPSR and C2H4/H2 pulse reaction over K-Fe-MnO/Si-2 catalysts clearly show that the K2O additive into Fe-MnO/Si-2 catalyst leads to a remarkable increase in both the capacity and strength of the strong CO ad-species that will produce much more |Cad| via their disproportionation at higher temperatures. This results in an increase in the CO conversion and the selectivity to light olefins, and a decrease in CH4 formation. Moreover, K2O can suppress the disproportionate of C2H4 that occurs during the reaction as a side-reaction Meanwhile, the MnO promoter mainly prohibits the hydrogenation of C2H4 and C3H6, which is favorable to enhancing the selectivity to C2H4 and C3H6 and decreasing the formation of C2H6, and C3H8. It is also of interest that MnO has har 相似文献
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lntroductionInordcrtoselcctivcl}'produccIightoIcfinsfroms}'ngas.thcbinderusedforimprovingthecatal}'ststrcngthshouldbcfavorabIcforprimary'formingofligl1tolcfinsfroms}ngasandforprohibitingsidereactionsoflightoIcfi.sIll.lthasbccnshownthattheundesirablcstrengthofsilicalitc-2zcolitccanbcimprovcdb}addingbindcrs.Hot`ycver.thcadditionofthcbinder`"illcauscsomcchangcsinthcph}'sical-chcmicalstatcofthecatal}ticactivemetalas``cllasitscatal}ticbcha.io,ll'2I.InourprcviouspaperTiO2wasprovedtobcadcsirablcbi… 相似文献
18.
《天然气化学杂志》1992,(2)
Microreactor-chromatography and XRD technique have been used to investigate the proper-ties of Ni/Al_2O_3 catalyst impregnated with rare earth oxides for the steam reforming of methane.Theresults of the study have shown that the stability of catalytic activity and the ability of resistance to ox-idation of high temperature steam are improved. 相似文献
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STUDY ON THE SURFACE MODIFICATION OF NANO-TiO2 BY GRAFTING PMMA/PBMA AND ITS THERMAL STABILITY 总被引:1,自引:0,他引:1
The surface of nano-TiO2 was encapsulated with hydroxyl-propyl-methyl cellulose (HPMC), and then cografted with acrylates. Conditions of absorbing and grafting have been studied. Modified nano-TiO2 particles were characterized by FT-IR spectra, TEM and TG analysis. It was convinced from FT-IR studies that both methyl methacrylate (MMA) and butylmethacrylate (BMA) were co-grafted onto the surface of nano-TiO2 particles. TEM images show that the surface of nano-TiO2 particles was successfully modified by a thick layer of film-like polymer. TG results demonstrate that the decomposition temperature of HPMC-g-PMMA/PBMA, which has been grafted onto the surface of nano-TiO2, is 56.9 K higher than that of HPMC-g-PMMA/PBMA. 相似文献