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在温和条件下,无需表面活性剂和超声处理,一步法剥离 MWW 硼硅酸盐层状沸石前体。

Single-step delamination of a MWW borosilicate layered zeolite precursor under mild conditions without surfactant and sonication.

机构信息

Department of Chemical and Biomolecular Engineering, University of California at Berkeley , Berkeley, California 94720, United States.

出版信息

J Am Chem Soc. 2014 Jan 29;136(4):1449-61. doi: 10.1021/ja410141u. Epub 2014 Jan 10.

DOI:10.1021/ja410141u
PMID:24345282
Abstract

Layered borosilicate zeolite precursor ERB-1P (Si/B = 11) is delaminated via isomorphous substitution of Al for B using a simple aqueous Al(NO3)3 treatment. Characterization by PXRD shows loss of long-range order, and TEM demonstrates transformation of rectilinear layers in the precursor to single and curved layers in the delaminated material. N2 physisorption and base titration confirm the expected decrease of micropore volume and increase in external surface area for delaminated materials relative to their calcined 3D zeolite counterpart, whereas FTIR and multinuclear NMR spectroscopies demonstrate synthesis of Brønsted acid sites upon delamination. Comparative synthetic studies demonstrate that this new delamination method requires (i) a borosilicate layered zeolite precursor, in which boron atoms can be isomorphously substituted by aluminum, (ii) neutral amine pore fillers instead of rigid and large quaternary amine SDAs, and (iii) careful temperature control, with the preferred temperature window being around 135 °C for ERB-1P delamination. Acylation of 2-methoxynaphthalene was used as a model reaction to investigate the catalytic benefits of delamination. A partially dealuminated delaminated material displays a 2.3-fold enhancement in its initial rate of catalysis relative to the 3D calcined material, which is nearly equal to its 2.5-fold measured increase in external surface area. This simple, surfactant- and sonication-free, mild delamination method is expected to find broad implementation for the synthesis of delaminated zeolite catalysts.

摘要

层状硼硅酸盐沸石前驱体 ERB-1P(Si/B = 11)通过使用简单的水合 Al(NO3)3 处理进行 B 位的同晶取代进行剥离。PXRD 表征显示长程有序性丧失,TEM 证明前驱体中的直线层转化为剥离材料中的单层和弯曲层。N2 物理吸附和碱滴定证实,与煅烧的 3D 沸石相比,剥离材料的微孔体积减小,外部表面积增加,而 FTIR 和多核 NMR 光谱证明剥离后形成了 Brønsted 酸位。比较合成研究表明,这种新的剥离方法需要 (i) 硼硅酸盐层状沸石前驱体,其中硼原子可以被铝同晶取代,(ii) 中性胺孔填充剂而不是刚性和大的季铵 SDA,以及 (iii) 仔细控制温度,ERB-1P 剥离的优选温度窗口约为 135°C。2-甲氧基萘的酰化被用作模型反应来研究剥离的催化优势。部分脱铝的剥离材料在其催化初始速率方面相对于 3D 煅烧材料提高了 2.3 倍,这几乎与其外部表面积增加 2.5 倍的测量值相等。这种简单、无表面活性剂和超声、温和的剥离方法有望广泛应用于剥离沸石催化剂的合成。

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