Synthesis of zeolite L crystals with different shapes

被引:25
作者
Ban, Takayuki [1 ]
Saito, Haruka [1 ]
Naito, Miyoshi [1 ]
Ohya, Yutaka [1 ]
Takahashi, Yasutaka [1 ]
机构
[1] Gifu Univ, Fac Engn, Dept Mat Sci & Technol, Gifu 50111, Japan
关键词
Zeolite L; hydrothermal synthesis; crystal morphology; triethanolamine;
D O I
10.1007/s10934-006-9016-z
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Zeolite L crystals were synthesized hydrothermally from aqueous mixtures of potassium hydroxide, metallic aluminum, and colloidal silica. The influence of hydrothermal conditions and the addition of triethanolamine (N(C2H4OH)(3); H(3)tea) upon the formation and shape of the resulting zeolite L crystals was examined. When the mixtures of KOH:Al:SiO2:H2O = 2.2 or 2.5:1.0:4.5:80 were hydrothermally treated at 130 or 175 degrees C, the zeolite L crystals had a columnar shape. Decrease in the added amount of KOH facilitated crystal growth in the axial direction, whereas a decrease in hydrothermal temperature inhibited it. For the synthesis using H(3)tea, a silica-rich starting composition of KOH:Al:SiO2:H2O:H(3)tea = 10:1.0:15:250:x and a hydrothermal temperature of 120 degrees C was used. When no H(3)tea was added, the obtained zeolite L crystals had an indistinct shape. H(3)tea addition at x = 2 led to the formation of zeolite L crystals with a well-defined, clam-like shape. The formation of the well-defined shape is due to the coordination of H(3)tea to aluminate ions. The starting composition has some influence on the formation of the clam-like shape. The zeolite L crystal morphologies obtained in this study ranged from stick-like shapes to clam-like ones. The length-to-diameter ratios ranged from 0.2 to 5.8.
引用
收藏
页码:119 / 126
页数:8
相关论文
共 32 条
[1]   HYDROTHERMAL CHEMISTRY OF SILICATES .14. ZEOLITE CRYSTALLISATION IN PRESENCE OF MIXED BASES [J].
AIELLO, R ;
BARRER, RM .
JOURNAL OF THE CHEMICAL SOCIETY A -INORGANIC PHYSICAL THEORETICAL, 1970, (09) :1470-&
[2]  
Ban T, 1999, ANGEW CHEM INT EDIT, V38, P3324, DOI 10.1002/(SICI)1521-3773(19991115)38:22<3324::AID-ANIE3324>3.0.CO
[3]  
2-J
[4]   Selective modification of the channel entrances of zeolite L with triethoxysilylated coumarin [J].
Ban, T ;
Brühwiler, D ;
Calzaferri, G .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (42) :16348-16352
[5]   CRYSTAL STRUCTURE OF SYNTHETIC ZEOLITE L [J].
BARRER, RM ;
VILLIGER, H .
ZEITSCHRIFT FUR KRISTALLOGRAPHIE KRISTALLGEOMETRIE KRISTALLPHYSIK KRISTALLCHEMIE, 1969, 128 (3-6) :352-&
[6]   PLATINUM-ZEOLITE INTERACTIONS IN ALKALINE L-ZEOLITES - CORRELATIONS BETWEEN CATALYTIC ACTIVITY AND PLATINUM STATE [J].
BESOUKHANOVA, C ;
GUIDOT, J ;
BARTHOMEUF, D ;
BREYSSE, M ;
BERNARD, JR .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1981, 77 :1595-1604
[7]   Injecting electronic excitation energy into an artificial antenna system through an Ru2+ complex [J].
Bossart, O ;
De Cola, L ;
Welter, S ;
Calzaferri, G .
CHEMISTRY-A EUROPEAN JOURNAL, 2004, 10 (22) :5771-5775
[8]   Molecular sieves as host materials for supramolecular organization [J].
Brühwiler, D ;
Calzaferri, G .
MICROPOROUS AND MESOPOROUS MATERIALS, 2004, 72 (1-3) :1-23
[9]   Host-guest antenna materials [J].
Calzaferri, G ;
Huber, S ;
Maas, H ;
Minkowski, C .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (32) :3732-3758
[10]   Photonic antenna system for light harvesting, transport and trapping [J].
Calzaferri, G ;
Pauchard, M ;
Maas, H ;
Huber, S ;
Khatyr, A ;
Schaafsma, T .
JOURNAL OF MATERIALS CHEMISTRY, 2002, 12 (01) :1-13