Molecular-sieving Separation of p-Xylene with Metal-organic Frameworks

IF 0.6 4区 工程技术 Q4 ENERGY & FUELS Journal of The Japan Petroleum Institute Pub Date : 2021-05-01 DOI:10.1627/JPI.64.147
A. Yonezawa, Naoki Tanaka, Yoshiki Hayase, M. Sano, Toshimitsu Suzuki, T. Miyake
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引用次数: 2

Abstract

Metal-organic frameworks (MOFs)1),2) have recently attracted much attention because of their unique properties such as crystalline and microporous structure, high thermal stability up to around 400 °C, and easy modification of pore structure and chemical properties3). Generally, MOFs consist of a multi-valent metal cation or cluster at the corner position and dior tri-carboxylic acids as the bridging unit (linker)2). MOFs with desired physical and chemical properties may be designed and synthesized by combining various metal cations and linkers. MOFs with unique properties have high potential for various applications such as adsorbents, membranes, sensors, catalysts, and others. In particular, MOFs are expected to act as lightweight hydrogen storage materials4)~6) due to their extremely high specific surface areas reaching 6000 m2 g1. Recently, MOFs have been widely studied as catalysts7),8). MOFs have also been evaluated for the separation of aromatics9),10) and aliphatic hydrocarbons11),12). p-Xylene is an important raw material for terephthalic acid, the co-monomer for polyethylene terephthalate. Nowadays, p-xylene is produced by separation from the xylene mixture by adsorption with zeolite13) or crystallization14). In the former method, xylenes diffuse into the micropores of zeolite and separation of p-xylene is based on the adsorption stability in the micropores. Multiple adsorption columns are needed for effective separation, and the feed flow is changed by the operation of many valves systematically (pseudo-transfer bed separation). Consequently, the separation process is complicated and the equipments are costly. In contrast, separation by crystallization necessitates heating and cooling of the vessel and so the energy consumption is high. Therefore, a new process to separate p-xylene at lower cost is very desirable. MOFs have been investigated for the separation of xylenes15)~25). In most cases, xylenes diffused into the micropores and separation was governed by the diffusion rate based on the molecular size of xylenes or by interactions between the MOF surface and xylenes. The separation mechanism is similar to that of the conventional process using zeolite, so the required volume of adsorbent is large because all the xylene substrate [Regular Paper]
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金属-有机骨架对二甲苯的分子筛分离
金属有机骨架(mof)1),2)由于其独特的性质,如晶体和微孔结构,高达400°C的高热稳定性,以及易于修饰的孔结构和化学性质3),近年来备受关注。一般来说,mof由位于角落位置的多价金属阳离子或簇组成,并以三羧酸作为桥接单元(连接剂)。通过组合各种金属阳离子和连接剂,可以设计和合成具有所需物理和化学性能的mof。mof具有独特的性能,在吸附剂、膜、传感器、催化剂等方面具有很大的应用潜力。特别是,由于mof具有高达6000 m2 g1的极高比表面积,因此有望作为轻质储氢材料(4)~6)。近年来,mof作为催化剂得到了广泛的研究[7],[8]。mof在分离芳烃(9)、10)和脂肪族烃(11)、12)方面也得到了评价。对二甲苯是生产聚对苯二甲酸的共聚单体对苯二甲酸的重要原料。现在,对二甲苯是通过沸石吸附或结晶从二甲苯混合物中分离出来的。在前一种方法中,二甲苯扩散到沸石的微孔中,对二甲苯的分离是基于微孔中的吸附稳定性。有效分离需要多个吸附塔,进料流量由多个阀门系统操作改变(伪传递床分离)。因此,分离过程复杂,设备昂贵。相反,结晶分离需要对容器进行加热和冷却,因此能耗很高。因此,寻找一种低成本分离对二甲苯的新工艺是非常必要的。研究了mof用于二甲苯(15)~25)的分离。在大多数情况下,二甲苯扩散到微孔中,分离由基于二甲苯分子大小的扩散速率或MOF表面与二甲苯的相互作用决定。该分离机理与使用沸石的常规工艺相似,由于全部采用二甲苯作为基材,因此所需吸附剂体积大。
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来源期刊
Journal of The Japan Petroleum Institute
Journal of The Japan Petroleum Institute 工程技术-工程:石油
CiteScore
1.70
自引率
10.00%
发文量
29
审稿时长
>12 weeks
期刊介绍: “Journal of the Japan Petroleum Institute”publishes articles on petroleum exploration, petroleum refining, petrochemicals and relevant subjects (such as natural gas, coal and so on). Papers published in this journal are also put out as the electronic journal editions on the web. Topics may range from fundamentals to applications. The latter may deal with a variety of subjects, such as: case studies in the development of oil fields, design and operational data of industrial processes, performances of commercial products and others
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