Kinetics of adsorptive desulfurization over alkaline-treated Beta zeolite

被引:0
|
作者
School of Chemical Engineering, Beijing University of Chemical Technology, Beijing [1 ]
100029, China
机构
来源
Huagong Xuebao | / 9卷 / 3747-3754期
基金
中国国家自然科学基金;
关键词
Sodium hydroxide - Pore size - Diffusion - Sulfur compounds - Desulfurization - Molecular sieves - Pore structure - Zeolites - Crystal structure - Sieves - Rate constants - Kinetics;
D O I
10.11949/j.issn.0438-1157.20160245
中图分类号
学科分类号
摘要
When molecular size of an adsorbate is as large as the pore size of molecular sieves, the adsorbate can enter into the pore structure and thus the pore size of molecular sieves is a critical factor in determining adsorption performance. To improve adsorbate selectivity and diffusion, Beta molecular sieves were modified by alkaline treatment of NaOH solution. The treated Beta molecular sieves were characterized by analytical techniques of BET, TEM, FT-IR, XRD and NH3-TPD to investigate the alkaline treatment process on crystal structure, surface acidity and pore structure. Adsorption desulfurization showed that both adsorption quantity and adsorption rate of alkaline-treated Beta molecular sieves were improved obviously. Especially the adsorption of large-kinetic-sized dibenzothiophene reached to 5.06 mg·g-1. The kinetics of adsorbing dibenzothiophene on Beta molecular sieves was a pseudo-2nd-order adsorption process. After alkaline treatment, rate constants of both adsorption and molecular diffusion inside pores were increased significantly, which in turn improved mass transfer of diffusion inside porous structures and desulfurization efficiency of sulfur compounds. © All Right Reserved.
引用
收藏
相关论文
共 50 条
  • [1] Adsorptive desulfurization over hierarchical beta zeolite by alkaline treatment
    Fuping Tian
    [J]. Journal of Energy Chemistry, 2012, (06) : 647 - 652
  • [2] Adsorptive desulfurization over hierarchical beta zeolite by alkaline treatment
    Tian, Fuping
    Yang, Xiaojian
    Shi, Yanchun
    Jia, Cuiying
    Chen, Yongying
    [J]. JOURNAL OF NATURAL GAS CHEMISTRY, 2012, 21 (06): : 647 - 652
  • [3] Catalytic cracking performance of alkaline-treated zeolite Beta in the terms of acid sites properties and their accessibility
    Tarach, K.
    Gora-Marek, K.
    Tekla, J.
    Brylewska, K.
    Datka, J.
    Mlekodaj, K.
    Makowski, W.
    Igualada Lopez, M. C.
    Martinez Triguero, J.
    Rey, F.
    [J]. JOURNAL OF CATALYSIS, 2014, 312 : 46 - 57
  • [4] Study of Isothermal Equilibrium, Kinetics and Thermodynamics of Adsorptive Desulfurization on Synthesized CuIYIIIY Zeolite
    Li Xiaojuan
    Song Hua
    Chang Youxin
    [J]. CHINA PETROLEUM PROCESSING & PETROCHEMICAL TECHNOLOGY, 2018, 20 (02) : 24 - 33
  • [5] Conversion of xylose to levulinic acid over modified acid functions of alkaline-treated zeolite Y in hot-compressed water
    Chamnankid, Busaya
    Ratanatawanate, Chalita
    Faungnawakij, Kajornsak
    [J]. CHEMICAL ENGINEERING JOURNAL, 2014, 258 : 341 - 347
  • [6] Study of Isothermal Equilibrium,Kinetics and Thermodynamics of Adsorptive Desulfurization on Synthesized Cu~ⅠY~ⅢY Zeolite
    Li Xiaojuan
    Song Hua
    Chang Youxin
    [J]. China Petroleum Processing & Petrochemical Technology, 2018, 20 (02) : 24 - 33
  • [7] Optimising the bioactivity of alkaline-treated titanium alloy
    Wei, M
    Kim, HM
    Kokubo, T
    Evans, JH
    [J]. MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS, 2002, 20 (1-2): : 125 - 134
  • [8] Adsorptive desulfurization over mesoporous materials
    Liu, Guozhu
    Shi, Yawei
    Zhang, Xiangwen
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2017, 253
  • [9] Adsorption of methylene blue on mesoporous carbons prepared using acid- and alkaline-treated zeolite X as the template
    Yan, Chunxiang
    Wang, Chongqing
    Yao, Jianfeng
    Zhang, Lixiong
    Liu, Xiaoqin
    [J]. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2009, 333 (1-3) : 115 - 119
  • [10] Adsorptive desulfurization on a heteroatoms Y zeolite prepared by secondary synthesis
    TANG Ke1
    2College of Petrochemical Engineering
    [J]. Science China Chemistry, 2010, (01) : 281 - 286