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JOURNAL OF MEMBRANE SCIENCE · 2025 · IF 9

Fabrication and characterization of polycrystalline MFI membranes on coarse macroporous supports for the separation of butane isomers

Hammad Saulat,Weiquan Feng,Zhongzhuang Hu,Mengxing He,Jinming Lu,Yan Zhang,Jianhua Yang,Cheng He

Separation of butane isomers holds substantial importance across various industrial sectors due to their divergent chemical characteristics and pervasive applications. Their efficient separation into high-purity iso-butane (i-C 4 ) and normal butane (n-C 4 ) allows their optimal utilization while maximizing economic benefit and minimizing waste, though their separation presents significant challenges due to their similar physicochemical properties and energy-intensive separation requirements. Polycrystalline zeolite-based membrane separation processes emerge as an energy-efficient approach for separating butane isomers by reducing the total operating energy consumption as compared to the conventional distillation process. However, the fabrication cost of polycrystalline zeolite membranes is high, predominantly dictated by the production cost of the support (≈ 50-70 %) rather than the polycrystalline zeolite layer. Herein, we report the fabrication of polycrystalline MFI membranes on inexpensive coarse macroporous α-Al 2 O 3 tube supports (symmetrical supports) with an average pore size in the range of 2 ∼ 3μm for separating butane isomers. Macroporous α-Al 2 O 3 tube supports are coated with single (sheet-like MFI crystals) and dual (sheet-like MFI crystals + MFI crystals) seed layers to achieve the desired separation performances. For coating a single seed layer, MFI nanocrystals were employed as precursors for synthesizing sheet-like MFI crystals with a high aspect ratio as compared to the conventional MFI crystals. Taking advantage of the high aspect ratio of sheet-like MFI crystals, single seed layer was fabricated on coarse macroporous α-Al 2 O 3 tube support, eliminating the time-intensive steps to reduce the support pore size and reducing the problem of pore plugging. Subsequently, a dual seed layer (sheet-like MFI crystals + MFI crystals) was also created by hot dip coating the MFI crystals on the surface of a single seed layer with the aim of fabricating a more compact, continuous, and molecular sieving polycrystalline MFI membrane with enhanced separation performance for the separation butane isomers. After hydrothermal crystallization, polycrystalline MFI membrane (M-2) fabricated on a single seed layer exhibits a separation factor and n-butane permeance of 33.80 and 2.00x10 -7 mol/m 2 .Pa.s, respectively. In contrast, the polycrystalline MFI membrane (D-3) formed on a dual seed layer demonstrates a separation factor and n-butane permanence of 40.60 and 1.47x10 -7 mol/m 2 .Pa.s, respectively. Both these membranes demonstrate good stability and reproducibility. Fabrication of polycrystalline MFI membranes on inexpensive coarse macroporous tube supports is a crucial advancement in reducing fabrication costs and facilitating industrial implementation. However, substantial potential remains for further scaling up and enhancing the separation performance of current polycrystalline MFI membranes.

研究领域: 材料科学 · 化学工程
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RSC Advances · 2018 ·Vol. 8 ·期 25 ·13728-13738 · IF 2.936

Dense and thin 13X membranes on porous α-Al2O3 tubes: preparation, structure and deep purification of oxygenated compounds from gaseous olefin flow

Yongxian Zhou,Wei Chen,Pengfei Wang,Yimin Zhang

The low contact efficiency, large mass transfer resistance and high operational cost of traditional 13X molecular sieve particle adsorbents (MSPs) have greatly limited their application in deep purification of trace oxygenated compounds from gaseous olefins. Herein, we successfully fabricated dense and thin 13X molecular sieve membranes on a porous α-Al2O3 tube (MSCMs) by a combination of 3-aminopropyl triethoxy silane (APTES) surface modification and vacuum pre-coating sol technology for purifying the above impurities. By a solid–solution transformation process, 13X molecular sieve membranes on MSCMs that were continuous and integral without any cracks, pinholes or other defects, and mainly composed of 1–1.5 μm regular 13X crystals with a thickness of 5–6 μm have been achieved. The purification performance of the MSPs, non-APTES functionalized MSCMs (nMSCMs) and MSCMs was evaluated by dynamic adsorption of N2 or C2H4 feed flow containing dimethyl ether, methanol and propanal impurities at room temperature. The results demonstrated that both the nMSCMs and MSCMs could deeply purify the trace amounts of the three oxygenated compounds to below 1 × 10−6 (mol mol−1) from gaseous olefins at an initial concentration of 20 × 10−6 (mol mol−1), exhibiting much more excellent purification performance than that of MSPs. In particular, the breakthrough times of MSCMs for dimethyl ether, methanol and propanal were 7 h, 32 h and 51 h in a N2 system, and 12.1 h, 53 h and 90 h in a C2H4 system. The cumulative adsorption amounts of MSCMs for dimethyl ether, methanol and propanal were 12.108 mg g−1, 35.812 mg g−1 and 103.129 mg g−1 in a N2 system, and 25.88 mg g−1, 94.19 mg g−1 and 256.26 mg g−1 in a C2H4 system, respectively. The regeneration experiment also indicated that the MSCMs had a more stable structure and a longer lifetime. The excellent purification performance of MSCMs could be attributed to the continuous 13X molecular sieve layers without non-adsorption interfacial voids. Hence, the MSCMs have great potential for future industrial application of trace oxygenated compound removal from gaseous olefins.

CAS / MDL: 919-30-2
研究领域: 化学工程 · 材料科学
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