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1.
在Silicalite-2分子筛担载的铁催化剂中添加MnO和K2O助剂,可显著提高其CO加氢制碳烯烃的选择性及催化活性,MnO助剂主要抑制乙烯和丙烯的加氢反应而提高烯/烷比值,K2O助剂则增加催化剂对CO的吸附能力,同时抑制乙烯在催化剂表二次反应(主要是乙烯的歧化反应),从而有利于提高低碳烯烃的选择性及催化剂活性。  相似文献   

2.
在Silicalite-2分子筛担载的铁催化剂中添加MnO和K2O助剂,可显著提高其CO加氢制低碳烯烃的选择性及催化活性.MnO助剂主要抑制乙烯和丙烯的加氢反应而提高烯/烷比值;K2O助剂则增加催化剂对CO的吸附能力,同时抑制乙烯在催化剂表面的二次反应(主要是乙烯的歧化反应),从而有利于提高低碳烯烃的选择性及催化剂活性.  相似文献   

3.
烯烃羰化一步制醇铑系催化新体系的研究   总被引:4,自引:0,他引:4  
羰基铑催化剂由于基加氢性能较弱,在羰基化反应的研究中,通常仅作为烯烃氢甲酰化制醛的催化剂。产物中得不到醇。本文则报道了以Rh2(AcO)4和Rh6(CO)16为催化剂,在一个反应器内进行烯烃氢甲酰化,加氢制醇的研究。系统考察了Rh/PBu2/EtOH催化体系受各种反应条件的影响。在最佳反应条件下,烯烃转化率达100%。对醇选择性亦在99.5%以上,正异构比在2以上。为烯烃一步制醇建立了铑系催化新体  相似文献   

4.
研究了FeCoMnK/BeO新型多组分催化剂上二氧化碳加氢的反应性能,考察了反应温度、空速及原料气组成对反应性能的影响。结果表明,二氧化碳的转化率及烯烃/烷烃比值均高于氧化铝、硅胶或活性炭担载的催化剂在647K,3000h^-1,CO2/H2体昆为1/3的条件下,低碳烯烃的收率最闹。利用原位FT-ER技术研究了该催化剂二氧化碳加氢反应的程序升温过程,提出了可能的反应机理。  相似文献   

5.
担载于Al2O3和ZrO2上的Fe(CO)9络合物的羰基在真空中极易脱附,在Ar或H2中250℃左右也可完全脱羰而成分散型催化剂。以ZrO2为载体者在Ar中低温下易发生表面岐化反应而生成CO2,高温下生成少量CH4。吸附于分散型催化剂上的CO在Ar或H2中均易发生岐化反应,以ZrO2为载体者在H2中发生加氢反应而生成CH4,在CO加氢中其反应物除了大量CO2外还有少量CH物。原位FT-IR谱表明以  相似文献   

6.
采用CO加氢反应、CO-TPD、CO/H2-TPSR及C2H2/H2-TPSR等手段,研究合成气制低碳烯烃反应K-Fe-MnO/MgO催化剂中MnO的助剂作用。结果表明MnO能大幅度提高低碳烯烃的选择性,尤其是乙烯的选择性;MnO能抑制催化剂表面的乙烯加氢,因而有利于提高低碳烯烃的选择性及烯/烷的比值。  相似文献   

7.
采用CO加氢反应、CO-TPD、CO/H_2-TPSR及C_2H_4/H_2-TPSR等手段,研究合成气制低碳烯烃反应K-Fe-MnO/MgO催化剂中MnO的助剂作用。结果表明MnO能大幅度提高低碳烯烃的选择性,尤其是乙烯的选择性;MnO能抑制催化剂表面的乙烯加氢,因而有利于提高低碳烯烃的选择性及烯/烷的比值。  相似文献   

8.
YBa2Cu3Ox(x=6-7)薄膜被合成在YSZ基底上,用FTIR,XPS,XRD等手段原位研究CO在薄膜上的吸附及加氢行为。CO吸附在Cu位置上,与YBCO体相中的O作用,生成表面CO2或-COO基团,导致YBCO中生产氧空位,使YBCO发生昌型转变,Cu^2+被还原为Cu^+或Cu^0.YBCO中的氧空位有利于CO、CO2及H2的吸附。CO、CO2在YBCO膜上的加氢产物为CH3OH、CH3  相似文献   

9.
碱土金属氧化物担载Fe-MnO催化剂可大幅度提高低碳烯烃的选择性和CO转化率,添加碱金属助剂将进一步改善其催化性能;MnO是铁催化剂由合成气制烯烃的有效助剂;碱土金属氧化物担体能抑制乙烯发生歧化反应及丙烯加氢反应,而MnO助剂主要抑制乙烯加氢反应,从而有利于提高合成气制低碳烯烃的选择性。  相似文献   

10.
Fe—Silicalite—2催化剂表面CO2加氢反应性能的研究   总被引:3,自引:0,他引:3  
研究了Fe/Silicalite-2催化剂CO2加氢低碳烯烃反应性能,利用CO2-TPD,CO2/H2-TPSR和CO/H2-TPSR表征手段,考察了铁含量及MnO助剂对Fe/Silicalite-2催化剂CO2吸附脱附及加氢反应性能的影响,表明随铁含量增加可提高催化剂对CO2的吸附能力,有利于提高CO2加氢反应的转化率。  相似文献   

11.
ThisprojectissllpportedbytheNationalNaturalScienceFotmdationofChina.IntroductionRecentstUdyonCOZhydrogenationfortheformationofhydrocarbonshascausedagreatinterest,especiallyintheproductionoflightalkenes.msreactionwillprovideanalternativeroutetoproducebasic…  相似文献   

12.
以乙烯为探针分子,采用TPSR手段研究催化剂担体对乙烯二次反应的影响。结果表明,担体的性质差异导致不同类型的乙烯二次反应,从而将直接影响到烯烃选择性。结果催化剂CO加氢反应结果及催化剂表面CO/H2-TPSR、C2H4/H27脉冲反应表征,发现担体的碱性促使乙烯歧化生成甲烷和丙烯,而担体的酸性促使乙烯歧化的同时,存在强烈的丙烯加氢作用,从而促进乙烯歧化,导致烯烃选择性大幅度下降,因而酸性担体不利于烯烃生成。  相似文献   

13.
K2O is a vital promoter to the Fe-MnO/silicalite-2 catalyst for light olefin formation from CO2 hydrogenation. With addition of it into the Fe-MnO/Si-2 catalyst the selectivity to light olefins increases greatly, while CH4 formation is inhibited evidently. Meanwhile, an obvious increment in CO2 conversion is also observed with the addition of K2O promoter. And it has been manifested that adding K2O to the Fe-MnO/Si-2 catalyst leads to remarkable increases in both the capacity and strength of the strong CO2 and CO adspecies. These produce much more[Cad] via their disproportionation at higher temperatures. This results in increase in the CO2 conversion and the selectivity to light olefins, and a decrease in CH4 formation.  相似文献   

14.
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   

15.
The performance of the K-Fe-MnO/Si-2 catalyst for the production of light olefins via Co hydrogenation changes obviously with the addition of binders. The results of CO hydrogenation. TPR, Mossbauer spectra CI0TPF, CO/H2-TPSR and C2H4/H2-TPSR are employed to investigate the effects of various binders on the physical-chemical states and catalytic behaviors of K-Fe-MnO/Si-2 catalyst to produce light olefins via syngas, TiO2 can promote the reduction of Fe and strengthen the adsorption of CO resulting in raising olefin selectivity. Other binders such as Al2O3, SiO2, MgO, once added into the catalyst, may cause formation of inorganic salts between FeO and Binders leading to a decrease of Fe reduction and a loss of olefin selectivity for CO hydrogenation. Especially, For K-Fe-MnO/Si-2 catalyst with Al2O3 binder directly, the strong secondary reactions of ethylene during CO hydrogenation cause a very poor light olefin selectivity, which will be improved greatly by modifying Al2O3.  相似文献   

16.
Intr0ductionRcccntl}.n1uchprogrcsshasbcc11n1adcinthcscIcctivcCOh\'drogcnationproducingliglltolcfinsvIas}'ngasb}'dct'clopingasilicalitc-2zcolitcsupp0rtcdFccatal\'st.Ithasbccllshox\llthatasilicaIitc-2zcoIitcsupportcdFccatal\'stpromotcdb}'aIkalin1ctalandMnOdispla}sadcsirabIcolcfil1sclccti\'it}(asl1ighas7()%)andadcsirablcCOcont'crsion(muchhighcrthan7O%)\\ithabett.,rcactionlifconst,ca.I1~31.Ho\\cvcr-thcundcsirablcstrcl1gthofSi-2zcolitcisunsuitabIcforitsapplicatiOninindustry-\\hichsIlouldbci…  相似文献   

17.
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.
High selectivity to light alkenes can be achieved from CO and CO_2hydrogenation over K-Fe-MnO/Si-2 catalyst.The alkene selectivity isinsensitive to reaction temperature for CO hydrogenation,while apparentlyincreases for CO_2 hydrogenation with raising reaction temperature.An increasein alkene selectivity is observed for both CO and CO_2 hydrogenation with GHSVrising,While a decrease with the elevation of reaction pressure for both CO/H_2and CO_2/H_2 reaction.A two-step mechanism is suggested forCO_2 hydrogenation to form hydrocarbons,by which the variations incontributions of CO and HC as products of CO_2/H_2 reaction with change ofreaction temperature,GHSV and pressure are explained.Moreover,thecatalyst is favorable for selective production of light olefins,which can alsoconcern the slightly secondary reactions of light olefins to some extent.  相似文献   

19.
IntroductionItilasbeenshot'-nthattileadditionofMnOpromotertoFocatal}stcanresultinaremarkableimprovementinthesclectivit}'to11ghtalkenesforCOh}!drogenationll'l.Ho-c'cvcr.thecadetofMnOonCH4formationandCOconversionisvery'ambigUouslltolMoreover.MnOpromotergrca…  相似文献   

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