Growth of zeolites A and X in low earth orbit

被引:18
作者
Warzywoda, J
Baç, N
Jansen, JC
Sacco, A [1 ]
机构
[1] Northeastern Univ, Dept Chem Engn, Ctr Adv Micrograv Mat Proc, Snell Engn Ctr 342, Boston, MA 02115 USA
[2] Delft Univ Technol, Fac Chem Technol & Mat Sci, NL-2628 BL Delft, Netherlands
基金
美国国家航空航天局;
关键词
crystal growth; hydrothermal synthesis; microgravity; zeolite A; zeolite X;
D O I
10.1016/S0022-0248(00)00659-X
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Zeolites A and X were grown hydrothermally in the microgravity environment (10(-3)-10(-6) g) of the space shuttle. It was hypothesized that this quiescent environment would lead to a means of producing "large" zeolite crystals having a high degree of crystalline perfection, and/or to a means of controlling defect concentration and location. Zeolite crystallizations have been carried out on four separate space shuttle missions: STS-40, USML-1, Spacehab-1, and USML-2. Preliminary results (STS-40) indicated that premixed solutions produced equal-sized intergrown crystals, and suggested that a "pre-nucleation" process had occurred before launch, All successive crystallizations were performed by mixing the precursor solutions on orbit, When nucleation was controlled using the aluminum complexing agents triethanolamine or 2, 2-bis(hydroxymethyl)-2,2', 2"-nitrilotriethanol, crystals synthesized in microgravity were similar to 25-70% larger in Linear dimension compared to their ground-based controls. The crystals grown in orbit had different nucleation/growth histories as indicated by their particle size distributions (PSDs). They frequently had different morphology (i.e., prominence of the {110} faces on zeolite A grown on earth vs, those grown in orbit) than did crystals grown from identical solutions, identically processed on earth. Based on the volume-normalized PSDs, similar to 15-40% fewer nuclei for zeolite A and similar to 40-60% fewer nuclei for zeolite X were observed in orbit, (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:140 / 149
页数:10
相关论文
共 19 条
[1]  
[Anonymous], 1996, CHEM WEEK, V158, P35
[2]  
BAUGHER CR, 1993, 31 AER SCI M EXH REN
[3]   CALIBRATION AND PERFORMANCE OF AN API AEROSIZER [J].
CHENG, YS ;
BARR, EB ;
MARSHALL, IA ;
MITCHELL, JP .
JOURNAL OF AEROSOL SCIENCE, 1993, 24 (04) :501-514
[4]   ZEOLITE SYNTHESIS IN UNSTIRRED BATCH REACTORS .1. NUCLEAR-MAGNETIC-RESONANCE IMAGING OF NONUNIFORM PRE-MIXING [J].
COKER, EN ;
HEES, PS ;
SOTAK, CH ;
DIXON, AG ;
THOMPSON, RW ;
SACCO, A .
MICROPOROUS MATERIALS, 1995, 3 (06) :623-636
[5]   THE INFLUENCE OF MICROGRAVITY ON ZEOLITE CRYSTALLIZATION [J].
DIRENZO, F ;
FAJULA, F ;
ESPIAU, P ;
NICOLLE, MA ;
DUTARTRE, R .
ZEOLITES, 1994, 14 (04) :256-261
[6]  
FISKE MR, 1992, 30 AER SCI M EXH REN
[7]   THE BEHAVIOR OF REGULAR-SHAPED NONSPHERICAL PARTICLES IN A TSI AERODYNAMIC PARTICLE SIZER [J].
MARSHALL, IA ;
MITCHELL, JP ;
GRIFFITHS, WD .
JOURNAL OF AEROSOL SCIENCE, 1991, 22 (01) :73-89
[8]   INVESTIGATIONS ON THE RELATIVE EFFECTIVENESS OF SOME TERTIARY ALKANOLAMINES IN THE SYNTHESIS OF LARGE-CRYSTAL ZEOLITE NAA [J].
MORRIS, M ;
DIXON, AG ;
SACCO, A ;
THOMPSON, RW .
ZEOLITES, 1993, 13 (02) :113-121
[9]   THE ROLE OF AN ALUMINUM-TERTIARY ALKANOLAMINE CHELATE IN THE SYNTHESIS OF LARGE CRYSTAL ZEOLITE NAA [J].
MORRIS, M ;
SACCO, A ;
DIXON, AG ;
THOMPSON, RW .
ZEOLITES, 1991, 11 (02) :178-183
[10]  
MULLIN JW, 1972, CRYSTALLIZATION, P21