4.7 Article

Conquering the solubility barrier of di-n-octylamine as structure-directing agent in hierarchical silicoaluminophosphate synthesis by using phase-transfer synthesis

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CHEMICAL ENGINEERING JOURNAL
卷 461, 期 -, 页码 -

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ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.141887

关键词

Organic structure -directing agent; Di; n -octylamine; Silicoaluminophosphate; Hydrophobic; SAPO-31; Hydroisomerization; N-dodecane

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The synthesis of SAPO-31 using a low-cost, barely soluble di-noctylamine as organic structure directing agent (OSDA) in a water/toluene biphasic media is reported. The resulting product is a hierarchically porous material built up of self-assembled nanocrystals with enhanced diffusion property and comparable acidity to a standard sample. The synthetic protocol expands the toolkit of candidate OSDAs and offers guidance towards manipulating hydroisomerization product slates.
Silicoaluminophosphates (SAPOs) are a class of microporous solids employed as solid acid catalysts or adsorbents in petrochemical and coal chemical processes, which are often generated in hydrothermal synthesis using watersoluble organic structure-directing agents (OSDA), resulting in the formation of micron sized, rod-like crystals running along pore-channel direction for unidimensional SAPOs. The use of a low-cost, barely soluble di-noctylamine (DOA) as OSDA in a water/toluene biphasic media to crystallize SAPO-31 is reported. The product is disclosed to be a hierarchically porous material built up of self-assembled nanocrystals (similar to 110 nm) with enhanced diffusion property and preserved acidity comparable to that of a standard sample derived using di-nhexylamine as OSDA. The formation is mediated by the formation of a Pickering emulsion structure that favors crystal nucleation over growth, thus overcoming the solubility barrier of candidate OSDA. The obtained material exhibited higher isomer yield in catalytic hydroisomerization of n-dodecane compared to the control sample. Product distribution analysis discloses that mono-branched isomers are generated mainly inside the micropores, while di-branched isomers are produced via key-lock catalysis on pore-mouth sites. The increase in isomerization selectivity is attributed to the formation of more mono-branched isomers and their lowered cracking probability associated with enhanced diffusion property. This new synthetic protocol expands the toolkit of candidate OSDAs towards hydrophobic molecules and exemplifies porogen-free fabrication of hierarchical SAPOs. The uncovered origin of shape-selectivity offers a guidance towards manipulating hydroisomerization product slates.

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