Reaction mechanism study of catalytic conversion of light straight-run naphtha to light olefins over micro-spherical HZSM-5 zeolite catalyst

被引:2
|
作者
Asfha, Hagos Birhane [1 ]
Berta, Ashenafi Hailu [1 ,3 ]
Kang, Nayoung [1 ]
Yun, Danim [1 ]
Park, Jaedeuk [1 ]
Park, Yong-Ki [1 ,2 ]
Kim, Kiwoong [1 ,2 ]
机构
[1] Korea Res Inst Chem Technol KRICT, Ctr Low Carbon Chem Proc, Gajeong Ro 141, Daejeon 34114, South Korea
[2] Univ Sci & Technol UST, Adv Mat & Chem Engn, Gajeong Ro 217, Daejeon 34113, South Korea
[3] Adama Sci & Technol Univ, Sch Mech Chem & Mat Engn, POB 1888, Adama, Ethiopia
关键词
Catalytic cracking; Naphtha cracking; Hydrocarbons; ZSM-5; catalyst; Reaction mechanism; N-BUTANE CRACKING; THERMAL-DECOMPOSITION; ORGANIC-COMPOUNDS; REACTION PATHWAYS; KINETIC-MODEL; FREE-RADICALS; ZSM-5; TRANSFORMATION; HYDROCARBONS; INTERCONVERSION;
D O I
10.1016/j.cattod.2023.114376
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Catalytic conversion of naphtha has attracted attention as an alternative method to the conventional thermal cracking to produce light olefins in an environment-friendly and energy-efficient way. In this work, a reaction mechanism study of light straight run naphtha cracking over micro-spherical catalyst containing HZSM-5 was systematically investigated using single hydrocarbon feeds, and the straight run naphtha itself. The identified reaction pathways from the single feeds along with the naphtha experimental data have been utilized to investigate reaction pathways of the naphtha conversion reactions. The experimental tests were carried out in the temperature ranges of 450-650 degrees C and space-times of 0.3-1.5 min using a fixed bed micro-reactor in isothermal and isobaric conditions. The product distribution for the naphtha feed shows that light paraffins and light olefins are the primary products, which are products of monomolecular protolytic cracking of the paraffin components of the naphtha feed. The olefin interconversion reactions illustrated that oligomerization and cracking by beta-scission dominate the secondary reactions of naphtha catalytic cracking conversions. The experiments con-ducted on cyclohexane, cyclohexene and n-hexane single feeds revealed that BTX formation proceeds through the formation of C6-C8 naphthenes, and C6-C8 cyclo-olefinic intermediates. Low temperatures and space times pro-mote the selectivity to propylene while the selectivity of ethylene increases with temperature. The degree of thermal cracking (DTC) illustrated that thermal cracking is considerable only for temperatures of higher than 550 degrees C.
引用
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页数:10
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