Synthesis of Zeolites via Interzeolite Transformations without Organic Structure-Directing Agents

被引:175
作者
Goel, Sarika [1 ]
Zones, Stacey I. [1 ]
Iglesia, Enrique [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
关键词
SEED-ASSISTED SYNTHESIS; FAU TYPE ZEOLITE; HYDROTHERMAL CONVERSION; CATALYSIS; CHA; MFI;
D O I
10.1021/cm504510f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report synthetic protocols and guiding principles inspired by mechanistic considerations for the synthesis of crystalline microporous solids via interzeolite transformations that avoid direct intervention by organic structure-directing agents. These protocols are specifically implemented to synthesize high-silica MFI (ZSM-5), CHA (chabazite), STF (SSZ-35), and MTW (ZSM-12) zeolites from FAU (faujasite) or BEA (beta) parent materials. These transformations succeed when they lead to daughter structures with higher framework densities, and their nucleation and growth become possible by the presence of seeds or of structural building units common to the parent and target structures, leading, in the latter case, to spontaneous transformations by choosing appropriate synthesis conditions. These protocols allow the synthesis of high-silica frameworks without the use of organic templates otherwise required. The NaOH/SiO2 ratio and Al content in reagents are used to enforce synchronization between the swelling and local restructuring within parent zeolite domains with the spoiling of fragments or building units from seeds of the target structure. Seed-mediated interconversions preserve the habit and volume of the parent crystals because of the incipient nucleation of the target structure at the outer regions of the parent domains. The pseudomorphic nature of these transformations requires the concurrent nucleation of mesopores within daughter zeolite crystals because their framework density is larger than that for the parent zeolites. The approach and evidence described shows, for the first time, that a broad range of zeolites rich in silica, and thus more useful as catalysts, can be made without the organic templates originally used to discover them.
引用
收藏
页码:2056 / 2066
页数:11
相关论文
共 43 条
  • [1] [Anonymous], 2008, Handbook of Heterogeneous Catalysis, V2nd edn
  • [2] [Anonymous], 2003, HDB ZEOLITE SCI TECH
  • [3] Baerlocher C., DATABASE ZEOLITE STR
  • [4] Barrer R. M., 1989, ACS SYM SER, V398, P11
  • [5] Calero S., 2010, MODELING TRANSPORT A, P335
  • [6] Issues in the synthesis of crystalline molecular sieves: Towards the crystallization of low framework-density structures
    Corma, A
    Davis, ME
    [J]. CHEMPHYSCHEM, 2004, 5 (03) : 304 - 313
  • [7] SHAPE-SELECTIVE CATALYSIS IN ZEOLITES
    CSICSERY, SM
    [J]. ZEOLITES, 1984, 4 (03): : 202 - 213
  • [8] The hydrothermal synthesis of zeolites: Precursors, intermediates and reaction mechanism
    Cundy, CS
    Cox, PA
    [J]. MICROPOROUS AND MESOPOROUS MATERIALS, 2005, 82 (1-2) : 1 - 78
  • [9] Zeolites from a Materials Chemistry Perspective
    Davis, Mark E.
    [J]. CHEMISTRY OF MATERIALS, 2014, 26 (01) : 239 - 245
  • [10] One-pot structural conversion of magadiite into MFI zeolite nanosheets using mononitrogen surfactants as structure and shape-directing agents
    Dhainaut, Jeremy
    Daou, T. Jean
    Bidal, Yannick
    Bats, Nicolas
    Harbuzaru, Bogdan
    Lapisardi, Gregory
    Chaumeil, Helene
    Defoin, Albert
    Rouleau, Loic
    Patarin, Joel
    [J]. CRYSTENGCOMM, 2013, 15 (15): : 3009 - 3015