scholarly journals Sandwich-Type Zeolite Intergrowths with MFI and the Novel Extra-Large Pore IDM-1 as Ordered End-Members

Author(s):  
Luis A. Villaescusa ◽  
Jian Li ◽  
Alvaro Mayoral ◽  
Zihao Rei Gao ◽  
Miguel A. Camblor
Membranes ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 86 ◽  
Author(s):  
Kyohei Ueno ◽  
Saki Yamada ◽  
Toshinari Watanabe ◽  
Hideyuki Negishi ◽  
Takuya Okuno ◽  
...  

Hydrophobic pure-silica *BEA-type zeolite membranes with large pores were prepared on tubular silica supports by hydrothermal synthesis using a secondary growth method and were applied to the separation of alcohol/water mixtures by pervaporation (PV), an alternative energy-efficient process for production of biofuels. Amorphous pure-silica tubular silica supports, free of Al atoms, were used for preparing the membranes. In this study, the effects of the synthesis conditions, such as the H2O/SiO2 and NH4F/SiO2 ratios in the synthetic gel, on the membrane formation process and separation performance were systematically investigated. The successfully prepared dense and continuous membranes exhibited alcohol selectivity and high flux for the separation of ethanol/water and butanol/water mixtures. The pure-silica *BEA membranes obtained under optimal conditions (0.08SiO2:0.5TEAOH:0.7NH4F:8H2O) showed high PV performance with a separation factor of 229 and a flux of 0.62 kg·m−2·h−1 for a 1 wt % n-butanol/water mixture at 318 K. This result was attributed to the hydrophobicity and large pore size of the pure-silica *BEA membrane. This was the first successful synthesis of hydrophobic large-pore zeolite membranes on tubular supports with alcohol selectivity, and the obtained results could provide new insights into the research on hydrophobic membranes with high permeability.


Polyhedron ◽  
2017 ◽  
Vol 133 ◽  
pp. 343-347 ◽  
Author(s):  
Dashuai Liang ◽  
Qin Wang ◽  
Huan Li ◽  
Hongxia Zhao ◽  
Zhengdong Yu ◽  
...  

2008 ◽  
Vol 80 (11) ◽  
pp. 2273-2282 ◽  
Author(s):  
Kyosuke Ito ◽  
Hui Jang ◽  
Koji Sakashita ◽  
Sachio Asaoka

The catalysts that can efficiently hydro-reform higher n-paraffin to lower isoparaffins for environmentally friendly gasoline were studied. The catalysts were examined by the conversion of n-hexadecane, n-C16H34 to i-C6H14~i-C12H26. The tri-modally nanoporous (nanometer-size) catalysts composed of (Ni-Mo)/[γ-Al2O3], nano-oxide, and nanocrystalline zeolite have some active and selective performances because of the cooperation between (Ni-Mo)/[γ-Al2O3] and the composite of nano-oxide-nanozeolite. The (Ni-Mo)/[γ-Al2O3] component holding the skeletal isomerization activity enhances the cracking activity on the composite of nanoporous (np)-Al2O3-USY (ultra-stable Y-type zeolite) to result in i-C6H14~i-C12H26 as the isomerization of n-hexadecane followed the cracking reaction. The catalyst composed of nanocrystalline BEA (beta-type zeolite) or MFI (ZSM-5-type zeolite) zeolite can be more activated with the nano-SiO2 than with the nano-Al2O3. The catalyst composed of the dealuminated zeolite, USY (SiO2/Al2O3 = 12) cannot be activated with the nano-SiO2 but with the nano-Al2O3. This activation depends on the SiO2/Al2O3 ratio of the USY. It is considered that the catalytic property of the three components is partially due to the novel active sites formed concertedly at the interface of the nano-oxides and the nanozeolites. The novel sites have a major role for the isomerization and cracking as the moderate and strong acids and are generated when Si-OH in the nanopores of the USY resulted from the dealumination catches Al-OH in the nano-Al2O3 to form Si-O-Al-O-Al-O-Si instead of Si-O-Al-O-Si-O-Si-O.


Author(s):  
Cong-Yan Chen ◽  
Larry W. Finger ◽  
Ronald C. Medrud ◽  
Charles L. Kibby ◽  
Peter A. Crozier ◽  
...  

2018 ◽  
Vol 22 (01n03) ◽  
pp. 243-249 ◽  
Author(s):  
Büşra Mızrak ◽  
Efe Baturhan Orman ◽  
Şaziye Abdurrahmanoğlu ◽  
Ali Rıza Özkaya

In this study, the novel Zn(II), metal-free and sandwich-type Lu(Pc)2 phthalocyanines containing tetra pyridine substituted at peripheral position were synthesized. All the new compounds have been characterized by FT-IR and UV-vis spectroscopy, [Formula: see text]H-NMR, MALDI-MS and elemental analysis. The electrochemical and spectroelectrochemical properties of all novel metallo- and metal free phthalocyanine compounds were also investigated by voltammetric and in situ spectroelectrochemical measurements on Pt in dimethylsulfoxide/tetrabutylammonium perchlorate.


Author(s):  
S. Ritchie ◽  
J. C. Bennett ◽  
A. Prodan ◽  
F.W. Boswell ◽  
J.M. Corbett

A continuous sequence of compounds having composition NbxTa1-xTe4; 0 ≤ x ≤ 1 have been studied by electron diffraction and microscopy. Previous studies have shown that the end members of the series, TaTε4 and NbTε4 possess a quasi-one-dimensional character and exhibit charge density wave (CDW) distortions. In these compounds, the subcell structure is tetragonal with axes (a × a × c) and consists of the metal atoms (Nb or Ta) centered within an extended antiprismatic cage of Te atoms. At room temperature, TaTε4 has a commensurate modulation structure with a 2a × 2a × 3c unit cell. In NbTε4, an incommensurate modulation with × ∼ 16c axes is observed. Preliminary studies of the mixed compounds NbxTα1-xTε4 showed a discontinuous jump of the modulation wave vector commensurate to incommensurate when the Nb dopant concentration x, exceeded x ≃ 0.3, In this paper, the nature of the compositional dependence of is studied in greater detail and evidence is presented for a stepwise variation of . This constitutes the first direct evidence for a Devil's staircase in CDW materials.


2010 ◽  
Vol 34 (8) ◽  
pp. S33-S33
Author(s):  
Wenchao Ou ◽  
Haifeng Chen ◽  
Yun Zhong ◽  
Benrong Liu ◽  
Keji Chen

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