Synthesis of ordered lamellar supermicroporous silica with rigid neutral and long-chain cationic composite templating route

被引:2
作者
Chen, Shangxing [1 ]
Wang, Peng [1 ]
Fan, Guorong [1 ]
Liao, Shengliang [1 ]
Si, Hongyan [1 ]
Wang, Zongde [1 ]
机构
[1] Jiangxi Agr Univ, Coll Forestry, Collaborat Innovat Ctr Jiangxi Typ Trees Cultivat, Nanchang, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
LIQUID;
D O I
10.1371/journal.pone.0216117
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Using a mixture of neutral primary amine dehydroabietylamine (DHAA) and long-chain cetyltrimethyl ammonium bromide (CTAB) as the template, ordered lamellar supermicroporous silicas were synthesized with NaOH as the base source and tetraethylorthosilicate (TEOS) as the silica source. The concentrations of DHAA, CTAB, and NaOH in the synthesis system had great effects on the structural properties of the samples. When the molar ratio of components was nTEOS:nCTAB:nDHAA:nNaOH:nH(2)O = 1:0.114:0.00457:0.5:60, the material showed a lamellar phase with the highest ordering degree. By adding only a trace amount of DHAA into the synthesis system, the structure of the samples could be transformed from cubic phase to lamellar phase, since the added DHAA solubilized in CTAB micelles to change the effective surfactant ion pair packing parameter. The dosage of CTAB should be moderate; too high or too low will decay the ordering degree of the lamellar structure. A much higher concentration of NaOH resulted in an ethanol-rich solvent in which the DHAA did not solubilize in the micelles of CTAB, but adsorbed at the hydrophilic headgroup-solvent interface. Accordingly, a structural transformation from lamellar phase to hexagonal phase occurred.
引用
收藏
页数:13
相关论文
共 21 条
[1]   Novel super-microporous silicate templating by ω-hydroxyalkylammonium halide bolaform surfactants [J].
Bagshaw, SA ;
Hayman, AR .
CHEMICAL COMMUNICATIONS, 2000, (07) :533-534
[2]  
Bagshaw SA, 2001, ADV MATER, V13, P1011, DOI 10.1002/1521-4095(200107)13:12/13<1011::AID-ADMA1011>3.0.CO
[3]  
2-T
[4]   MOLECULAR OR SUPRAMOLECULAR TEMPLATING - DEFINING THE ROLE OF SURFACTANT CHEMISTRY IN THE FORMATION OF MICROPOROUS AND MESOPOROUS MOLECULAR-SIEVES [J].
BECK, JS ;
VARTULI, JC ;
KENNEDY, GJ ;
KRESGE, CT ;
ROTH, WJ ;
SCHRAMM, SE .
CHEMISTRY OF MATERIALS, 1994, 6 (10) :1816-1821
[5]   A NEW FAMILY OF MESOPOROUS MOLECULAR-SIEVES PREPARED WITH LIQUID-CRYSTAL TEMPLATES [J].
BECK, JS ;
VARTULI, JC ;
ROTH, WJ ;
LEONOWICZ, ME ;
KRESGE, CT ;
SCHMITT, KD ;
CHU, CTW ;
OLSON, DH ;
SHEPPARD, EW ;
MCCULLEN, SB ;
HIGGINS, JB ;
SCHLENKER, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10834-10843
[6]   From microporous to mesoporous molecular sieve materials and their use in catalysis [J].
Corma, A .
CHEMICAL REVIEWS, 1997, 97 (06) :2373-2419
[7]   Ordered porous materials for emerging applications [J].
Davis, ME .
NATURE, 2002, 417 (6891) :813-821
[8]   Shape selectivity extending to ordered supermicroporous aluminosilicates [J].
Fu, Wen Hua ;
Liang, Xiao Min ;
Zhang, Haidong ;
Wang, Yi Meng ;
He, Ming Yuan .
CHEMICAL COMMUNICATIONS, 2015, 51 (08) :1449-1452
[9]   Highly ordered supermicroporous aluminosilicates with cubic Pm3n symmetry fabricated in weakly acidic solution [J].
Fu, Wen Hua ;
Wang, Yi Meng ;
He, Ming Yuan .
RSC ADVANCES, 2013, 3 (40) :18519-18528
[10]   Surfactant control of phases in the synthesis of mesoporous silica-based materials [J].
Huo, QS ;
Margolese, DI ;
Stucky, GD .
CHEMISTRY OF MATERIALS, 1996, 8 (05) :1147-1160