Hexane activation over vanadium modified zeolite ZSM-5

被引:4
作者
Naicker, T. [1 ]
Friedrich, H. B. [1 ]
机构
[1] Univ KwaZulu Natal, Sch Chem, ZA-4041 Durban, South Africa
关键词
Hexane activation; ZSM-5; Vanadium modified zeolite; SELECTIVE OXIDATION; N-HEXANE; CATALYTIC-PROPERTIES; OXIDE CATALYSTS; OXYDEHYDROGENATION; DEHYDROGENATION; PROPANE; ACID; SPECTROSCOPY; CONVERSION;
D O I
10.1007/s10934-012-9651-5
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The influence on the form of ZSM-5, vanadium content and the elimination of the exterior surface, on the activity and selectivity of n-hexane oxidation was studied using a fixed bed reactor. Blank reactor studies (carborundum packed reactor) showed no conversion below 450 A degrees C with the highest conversion (8 %) at 500 A degrees C. The dominant products were found to be carbon oxides (Sel./% = 90) with minor selectivities to the hexene isomers (7 %) with the remainder being cracked products, THF and benzene. H-ZSM-5 with different SiO2/Al2O3 ratios (100 and 320) and Na-ZSM-5 (SiO2/Al2O3 ratio of 100) were tested under non-oxidative conditions. As the ratio of the SiO2/Al2O3 increased the aluminium content decreases and so too does the cracking ability of the zeolite (i.e. yield of cracked products dropped from 36 to 8 %). However, the use of the Na- form of the ZSM-5 zeolite completely eliminated acid cracking and therefore this system was further investigated. Na-V-ZSM-5 (similar to 1 % loading) was synthesized using the solid state ion-exchange method. Time on stream experiments (fresh batch of catalyst for each experiment with sampling at the same time for a period of 24 h) were conducted and temperature (350, 400 and 450 A degrees C), contact time (0.5, 0.8, 1.1 and 1.5 s) and fuel/air ratios (0.7, 1.3 and 2) were varied. The optimum conditions (Conv./% = 39) for terminal functionalised products were found to be at 400 A degrees C at a contact time of 1.1 s and a fuel air ratio of 1.3. With the lower fuel air ratio of 0.7 (oxygen rich conditions), hexanal formation was favoured.
引用
收藏
页码:763 / 775
页数:13
相关论文
共 48 条
  • [1] ALBONETTI S, 1996, CATAL REV SCI ENG, V38, P414
  • [2] Armor J.N., 1994, STUD SURF SCI CATAL, V92, P51
  • [3] Structure and catalytic properties of VOx/MCM materials for the partial oxidation of methane to formaldehyde
    Berndt, H
    Martin, A
    Brückner, A
    Schreier, E
    Müller, D
    Kosslick, H
    Wolf, GU
    Lücke, B
    [J]. JOURNAL OF CATALYSIS, 2000, 191 (02) : 384 - 400
  • [4] Dehydrogenation and oxydehydrogenation of paraffins to olefins
    Bhasin, MM
    McCain, JH
    Vora, BV
    Imai, T
    Pujadó, PR
    [J]. APPLIED CATALYSIS A-GENERAL, 2001, 221 (1-2) : 397 - 419
  • [5] Oxidative dehydrogenation of short chain alkanes on supported vanadium oxide catalysts
    Blasco, T
    Nieto, JML
    [J]. APPLIED CATALYSIS A-GENERAL, 1997, 157 (1-2) : 117 - 142
  • [6] Cracking of pentenes to C2-C4 light olefins over zeolites and zeotypes -: Role of topology and acid site strength and concentration
    Bortnovsky, O
    Sazama, P
    Wichterlova, B
    [J]. APPLIED CATALYSIS A-GENERAL, 2005, 287 (02) : 203 - 213
  • [7] Bulánek R, 2004, POL J CHEM, V78, P149
  • [8] Carlsson AF, 1996, J CATAL, V176, P459
  • [9] Some aspects that affect the selective oxidation of paraffins
    Cavani, F
    Trifiro, F
    [J]. CATALYSIS TODAY, 1997, 36 (04) : 431 - 439
  • [10] VANADIUM-ZEOLITE CATALYSTS FOR THE AMMOXIDATION OF XYLENES
    CAVANI, F
    TRIFIRO, F
    JIRU, P
    HABERSBERGER, K
    TVARUZKOVA, Z
    [J]. ZEOLITES, 1988, 8 (01): : 12 - 18