Catalytic cracking of n-hexane for producing light olefins on 3D-printed monoliths of MFI and FAU zeolites

被引:73
|
作者
Li, Xin [1 ]
Li, Wenbin [2 ]
Rezaei, Fateme [1 ]
Rownaghi, Ali [1 ]
机构
[1] Missouri Univ Sci & Technol, Dept Chem & Biochem Engn, Rolla, MO 65409 USA
[2] Missouri Univ Sci & Technol, Dept Mech & Aerosp Engn, Rolla, MO 65409 USA
关键词
3D printing; HZSM-5; monolith; HY monolith; n-Hexane cracking; Light olefins; SAPO-34; growth; COKE FORMATION; ACID SITES; SELECTIVE FORMATION; ZSM-5; ZEOLITES; BETA-ZEOLITE; CRYSTAL SIZE; PERFORMANCE; HYDROCARBONS; HEPTANE; DEHYDRATION;
D O I
10.1016/j.cej.2017.10.001
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Three dimensional (3D) printing manufacturing has attracted growing interests for material synthesis applied in various fields because of its rapid accomplishment, cost effectiveness, approach facilities and structure controllability. In this work, we present a facile and efficient method for the fabrication of 3D-printed HZSM-5 and HY monoliths with macro-meso-micorporosity as the heterogeneous catalysts for n-hexane cracking reaction. To modify and improve the performance of the monolithic catalysts, the silicoaluminophosphate with chabazite framework (SAPO-34) was grown on the zeolite monolith surface via secondary growth method. Characterization of the catalysts suggest that surface area, porosity, acidity and structure of the catalysts were influenced by both formulation into monolithic structures and growth of SAPO-34. The performance of the 3D-printed monolithic catalysts was investigated in catalytic cracking of n-hexane at 600 and 650 degrees C for 24 h time on stream. Our results indicated that HZSM-5 zeolite monolith exhibits more stable activity in n-hexane cracking and higher selectivity to light olefins than its powder counterpart. A highest selectivity to light olefins (53.0%) was found on HZSM-5 zeolite monolith at 650 degrees C whereas over HY zeolite monolith the highest selectivity was found to be 57.9% at 600 degrees C. SAPO-34 growth enhanced the activity all monolithic catalysts and significantly improved catalytic selectivity to BTX (benzene, toluene and xylene) over HY monoliths. The highest BTX selectivity reached 27.5% on SAPO-34 coated HY monolith at 600 degrees C.
引用
收藏
页码:545 / 553
页数:9
相关论文
共 50 条
  • [1] Catalytic cracking of n-hexane for producing propylene on MCM-22 zeolites
    Wang, Yong
    Yokoi, Toshiyuki
    Namba, Seitaro
    Kondo, Junko N.
    Tatsumi, Takashi
    APPLIED CATALYSIS A-GENERAL, 2015, 504 : 192 - 202
  • [2] Synthesis of Cr, Cu, Ni, and Y-Doped 3D-Printed ZSM-5 Monoliths and Their Catalytic Performance for n-Hexane Cracking
    Li, Xin
    Alwakwak, Abdo-Alslam
    Rezaei, Fateme
    Rownaghi, Ali A.
    ACS APPLIED ENERGY MATERIALS, 2018, 1 (06): : 2740 - 2748
  • [3] Temperature programmed desorption of n-hexane and n-heptane from MFI and FAU zeolites
    Makowski, Waclaw
    Majda, Dorota
    JOURNAL OF POROUS MATERIALS, 2007, 14 (01) : 27 - 35
  • [4] Temperature programmed desorption of n-hexane and n-heptane from MFI and FAU zeolites
    Wacław Makowski
    Dorota Majda
    Journal of Porous Materials, 2007, 14 : 27 - 35
  • [5] Selective Production of Light Olefins from Catalytic Cracking of n-Hexane over OSDA-Free Beta Zeolites
    Wang, Yong
    Otomo, Ryoichi
    Tatsumi, Takashi
    Yokoi, Toshiyuki
    CATALYSIS SURVEYS FROM ASIA, 2016, 20 (01) : 1 - 12
  • [6] Selective Production of Light Olefins from Catalytic Cracking of n-Hexane over OSDA-Free Beta Zeolites
    Yong Wang
    Ryoichi Otomo
    Takashi Tatsumi
    Toshiyuki Yokoi
    Catalysis Surveys from Asia, 2016, 20 : 1 - 12
  • [7] Study on Catalytic Performance of Nanosheet MFI Structured Zeolite in n-Hexane Cracking
    Ji, Yajun
    Yang, Honghui
    Yan, Wei
    Shiyou Xuebao, Shiyou Jiagong/Acta Petrolei Sinica (Petroleum Processing Section), 2018, 34 (05): : 1013 - 1019
  • [8] Crystal size of MFI-type zeolites for catalytic cracking of n-hexane under reaction-control conditions
    Nakasaka, Yuta
    Okamura, Takuya
    Konno, Hiroki
    Tago, Teruoki
    Masuda, Takao
    MICROPOROUS AND MESOPOROUS MATERIALS, 2013, 182 : 244 - 249
  • [9] Deactivation mechanism of MFI-type zeolites by coke formation during n-hexane cracking
    Nakasaka, Yuta
    Nishimura, Jun-ichi
    Tago, Teruoki
    Masuda, Takao
    CHEMICAL ENGINEERING JOURNAL, 2015, 278 : 159 - 165
  • [10] Deactivation mechanism of MFI-type zeolites by coke formation during n-hexane cracking
    Nakasaka, Yuta (nakasaka@eng.hokudai.ac.jp), 1600, Elsevier B.V., Netherlands (278):